http://www.HalloLondon.co.uk/ en-GB Here is the main description Thu, 29 Mar 2007 18:18:00 GMT 240 58 http://www.hallolondon.co.uk http://www.hallolondon.co.uk/gfx/logo_bw.gif Job duration: perm Start date: asap Description: For my client, an international, well-established Clinical Research Organisation with headquarters based in Reading area, I am currently looking for a number of experienced Clinical Research Associatesto join their hugely successful team working on various international clinical trials. Working as a CRA you will be mainly responsible for monitoring on every stage of the trial, investigators recruitment, study budget negotiations and reviewing clinicaldocuments. A full job description will be provided upon application. Candidates will need to be experienced Clinical ResearchAssociates with UK-based clinical monitoring experience. They will also need to be located within commutable distance from Reading or be prepared to relocate and speak fluent English. In return my client offers a very competitive basic salary combined with numerous benefits, dedicated training scheme and a great working environment. Due to company's continuous expansion ideal candidates will be offered a chance to progress within the organisation. For more information, full job description and for an immediate consideration please forward your CV to Agata on agata.lugowska@secpharma.com or call 0044 (0) 2072556600 Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: clinical, monitoring Job Reference: 1200657 http://www.hallolondon.co.uk/index.html?op=3&id=532103 Job duration: Start date: ASAP Description: ## THIS POSITION CAN BE BASED IN EITHER PARIS or SOUTH SWITZERLAND ## Responsibilities: Pharmacovigilance Ensure regulatory compliance with worldwide Pharmacovigilance regulations Medical Case Assessment Case narrative writing MedDRA coding Ensure compliance with Eudravigilance reporting requirements Case follow up with health professional if needed Alert reporting to all competent Authorities Periodic Safety Report writing (PSUR, ASR�) Medical advice to fellow staff members and clients Provide medical expertise during review of clients medical documents Business Development and Pre Projects Participate in Pre Project for Pharmacovigilance proposals QA Pharmacovigilance Quality policy validation Participate in Pharmacovigilance technical procedures design and implementation Maintain Pharmacovigilance Technical procedures up to date Validating external translations order Industry: Science and Research Salary currency: gbp Salary Benefits: Benefits Salary: €80000 - €120000 per annum + Benefits Job type: Permanent Job skills: Pharmacovigilance, Drug Safety, Director Job Reference: 1007-143 http://www.hallolondon.co.uk/index.html?op=3&id=531914 Job duration: 3 months Start date: ASAP Description: Our client in Bedfordshire is looking for a Medical Affairs Scientist to join their exciting team on a 3 months contract. The ideal candidate must come from a Scientific Advisor background and also have good knowledge of Psychiatry. Purpose: �To be the Therapy Area scientific expert delivering medical insight and governance into the Brand, in order to meet Brand and Therapy Area (Psychiatry) objectives through Medical Excellence �Responsible for developing, maintaining, communicating and driving intelligent compliance of the Brand claims plan and current claims document �Responsible for technical input into concept development of Brand promotional material, and also for final signatory responsibilities where appropriate �Provide data and insight for enhancing promotionalmaterial through the offering development cycle �Liaise with Global to influence Brand core claims �Contribute to the development and execution of Medical Brand Plans to support Brand objectives "Check and approve promotional material for factual accuracy and review for Code compliance in line with Promotional Copy Approval process "Responsible for preparing and maintaining Data on File for the UK market "Responsible for clinical input into development of the risk minimisation plan for the brand as appropriate "Lead in preparing the medical case for the defence / challenge of promotional activities for ABPI when necessary appropriate "Prepare internal briefing documents for therapy area as required "Reply to "Horizon Scanning" requests for Development Product#s# "Provide support to Medical Information Adviser team when answering customer queries for products not covered by the EU MI team "Prepare brand and commercial product#s# notifications in line with commercial strategy "In line with MSLE team, visit external customers to resolve clinical/technical queries "Customer field contact according to therapy area demand "Develop & leverage medical insight through attendance at scientific meetings to further develop own knowledge base but in line with clear business need "Lead the development of clinical summaries for Medical Affairs, Brand Team andField Force from key relevant recently published papers "Provide support to the training manager on delivery of training on relevant scientific knowledge relevant to the brand "Responsible for providing therapy area technical and clinical input into Market Access submissions as required, in-line with overall brand strategy "In line with clear business need support the Sales Force at key national/local meetings "Lead the development and implementation of Clinical Advisory Boards in line with businessneed "Develop and maintain scientific relationships with key physicians to build customer insight and develop strategic partnerships as appropriate "Visit external customers to resolve clinical/technical queries and according to therapy area demand "Support sales force by responding to requests for scientific exchange of information from external customers and at key internalmeetings "Develop and leverage technical insight from external and internal customers into the Medical and Therapy Area plans"Support the delivery of key existing and emerging Life Cycle initiatives #MC3 etc.# by providing expert medical advice and customer insight as appropriate "Support media communications from the brand "Drive intelligent compliance through adherence tothe 2008 ABPI Code of Practice "Support the dissemination of Brand and disease area knowledge across the UKMC in accordance with business priorities "Regular communication of best practice and facilitation of knowledge sharing "Responsible for the training on the use of current claims document for originators within brand "Deputise for the Medical Leader as and when appropriate "Input into Medical Affairs Therapy Area Team performance metrics Essential: Life science degree or appropriate professional qualifications Desirable: Healthcare professional qualification e.g. Nurse, Pharmacist; PhD in relevant subject oStrongly preferred technical expertise in the allocated disease/therapy area - Psychiatry oProven expertise in the ABPI Code ofPractice oProven communication skills oPrior experience of commercially orientated positions oAwareness of NHS customer groups and other key customers EXPERIENCE & TRACK RECORD Essential: oSignificant experience in the pharmaceutical industry oProven ability to interact with external customers oExperience in medical writing oExperience of cross-functional team working Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £250 - £265 per day Job type: Contract Job skills: Medical Affairs,ScientificAdvisor Psychiatry, ABPI Code of Practice Job Reference: KP1007-134 http://www.hallolondon.co.uk/index.html?op=3&id=531346 Male and female escorts required.All ages,looks and types required with flexible hrs to suit YOU.No experience required for an IMMEDIATE start call 01484502774 or 07717411518. LIMITED PLACES ONLY! http://www.hallolondon.co.uk/index.html?op=3&id=525207 Job duration: perm Start date: asap Description: For my client, one of the most successful full-service international Clinical Research Organisations I am currently looking for a late phase Senior Clinical Site Coordinator to join their hugely successful team in West London. On this position you will be mainly responsible for assisting with the implementation of studies, recruitment and qualification of the study sites, training of sites on study protocol, guidelines, operations, anddata submission, preparation of study materials which may include protocol, questionnaires, case report forms, consent forms, newsletters, reports, etc as well as conveying project information and follow up on study progress with sites. An ideal candidate for this full-time permanent position will be an experienced Clinical Research Associate who would have experience and sound knowledge of late phase of clinical trials. They will ideally have previous clinical research monitoring experience gained in theUK. This opportunity will also suit Senior CRAs who are looking to take another step in their career and get involved in project management responsibilities. Clinical Research Professionals who wish to be mainly office-based with no need to travel to thesites would also be interested in this role which offers a great work-life balance. Since it is an office based position candidates will need to located within a commutable distance to West London or be willing to relocate if offered a role. In return myclient offers a permanent opportunity with a dedicated training scheme and an opportunity to grow within the organisation. Verycompetitive salary package combined with exceptional benefits scheme and a fantastic working environment are also offered for the right candidate. For a detailed job description an immediate consideration and more information about the opportunity pleaseforward your CV to agata.lugowska@secpharma.com or call Agata on (0) 2072556600 Industry: Science and Research Salary currency: gbp Salary Benefits: negotiable+benefits Salary: £40000 - £45000 per annum + negotiable+benefits Job type: Permanent Job skills: clinical, coordinator, cra, scra Job Reference: 1200065 http://www.hallolondon.co.uk/index.html?op=3&id=523097 Job duration: Permanent Start date: ASAP Description: Our client looking for a Clinical Feasibility Specialist II to join their teams on a permanent based in both Middlesex, UK and Germany. Essential Function Provide feasibility assessments for new business opportunities or awarded studies including supervision of external investigator surveys and coordination of other support groups as required. Develop operational strategies including scenario planning (country/site optimization) and support the preparation of bid defense meetings. Provide expertise in the recruitment and selection of qualified investigators in support of clinical projects by data mining internal data assets and using external data if appropriate. Working in close collaboration withlocal Clinical Trial Specialists staff in various countries. Contribute to strategies to improve the customer relationship withsites, including development of new models of collaboration. Analyze and work to continuously improve predictive investigator performance metrics. Key Accountabilities �Assume the ability to meet the requirements of a CFS I with a high degree ofproficiency and autonomy �Perform feasibility assessment of clinical protocols to assess the operational impact by theprotocol design, interpretation of past performance data and it�s relevance to the current protocol, coordinate the inputfrom other expert groups (Medical Services, Study Start-Up, Regulatory Affairs and Patient Recruitment Strategy Group) into thefeasibility assessment that is being delivered to the proposal writer �Develop recommendations for country allocation and site distribution inclusive of scenario planning by using the SPARC application �Develop feasibility and site selection slides with the support of Clinical Feasibility Specialist I in case of external survey for presentation at the bid defense meeting �Support the development of the proposals and costing for stand-alone Feasibility & Clinical Informatics services including proposal revisions as needed and contract review �Provide work instructions and guidance to Clinical Feasibility Specialist I & II and Clinical Informatics Specialists I & II for the conduct of questionnaire-based investigator surveys. �Perform quality review of feasibility/pre-qualification questionnaires and related reports/slides presentingthe survey results. �Prepare site lists by using data mining of internal and external data assets, using investigator performance data �Develop and support the implementation of site selection strategies in support of clinical projects in close collaboration with Clinical Trial Specialists in various countries and project teams. �Develop and implement strategies for improving investigator relationship management including new ways to collaborate with investigators, SMOs and otherinvestigator organisations. �Analyze and work to continuously improve predictive investigator performance metrics in support of site selection. �Assist in the development of programs to recruit and maintain a qualified pool of investigatorsin support of projects in all therapeutic areas. �Attend client meetings on an ad hoc basis �Keep manager informed about work progress and any issues to avoid surprises. Requires some interaction / supervision by Manager or assigned mentorSkills �Sense of urgency, initiative, and diplomacy �Strong analysis and synthesis skills �Working knowledge of worldwide clinical research �Sound interpersonal, verbal and written communication skills �Ability to manage multiple tasks with enthusiasm and prioritise workload with attention to detail Education �Educated to a degree in Science, possibly in Life Sciences, or relevant qualification/experience �Significant experience in clinical research within a CRO including appropriate expertise in feasibility assessments and/or clinical monitoring study coordination and/or site and investigator relationships Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Clinical, Feasibility Job Reference: KP1004-76 http://www.hallolondon.co.uk/index.html?op=3&id=522845 Job duration: 4 months Start date: August 2010 Description: Our client in Buckinghamshire is looking for a Drug Safety Associate to jointheir team on a 4 months contract. The ideal candidate must have a minimum of 18 months Drug Safety experience Responsiblefor the receipt and data entry of adverse event reports following Company Standard Operating Procedures, internal business practices and regulatory guidance documents to ensure compliance with worldwide safety regulations and corporate policies. Case Processing: Definition: The completion of full case information on the database, culminating in Quality Review to ensure accuracy and completeness. Activities Include: * Triage of incoming cases to determine seriousness for prioritisation of daily workflow (to be discussed re triage specialist) * Confirmation of Safety Co-ordinator case registry data * Database searches asnecessary * Completion of literature searches as necessary * Completion of remaining case data entry, including narrative or auto-narrative * Completion of risk and quality (label, approval, manual coding & quality review steps * Clarificationof unclear or illegible information from the LSO or Call Centre * Discuss source documents, coding conventions and ad-hoc queries with Medical Assessment Physician * Completion of protocol request forms as necessary * Preparation of deviation memo as necessary * Request deletions as necessary * Single case unblinding Processes and Procedures: Definition: Continuingawareness of company procedures and guidelines to maintain regulatory compliance. Activities Include: * Standard OperatingProcedures and Working Practices * Department guidance documents * MedDRA coding dictionary and MedDRA points to consider* Understand relevant safety implications regarding contracts with operating companies and/or marketing partners * Review andmake suggestions for system and procedure enhancements. Project Work Audits, Inspections and other Ad-hoc Requirements: Definition: Participation in projects, preparations for audits and inspections. Activities Include: * Participation in inspections and audits, as required (e.g., interviews) * Participation in local or global project teams Requirements/Skills Registered Nurse and/or Health/Biomedical Degree oPharmaceutical industry experience desired Required Skills/Abilities oIntermediateInformation Technology Skills oData entry experience desired oAccountability for delivery of results oDecision making skills oProblem solving skills oProactive approach/uses own initiative oManaging own work, ability to prioritize, plan and organize workassignments and work under strict timelines oAbility to follow guidelines, working practices etc. Experience of working with SOP/SWP's preferred oQuality orientation, attention to detail/accuracy oFlexibility/Adaptability oPositive attitude oGood team player oAbility to work independently and to collaborate oGood written and verbal communication skills -Understanding of medical terminology oAbility to summarize medical information Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £25 - £27 per hour Job type: Contract Job skills: case processing, AdverseEvents, Drug Safety Job Reference: KP1007-39 http://www.hallolondon.co.uk/index.html?op=3&id=521051 Job duration: Permanent Start date: ASAP Description: Our global client in Switzerland is looking for a Brand Safety Leader tojoin their expanding team on a permanent basis. Job Description : Serves as scientific safety leader for assigned projects/products . Once the project team is formed, responsible for the integration, analysis, and interpretation of safety information from all sources, including preclinical through lifecycle management (postapproval) and externally. 1. Responsible for safetyissue management from end of Phase I (POC) through Life Cycle Man-agement. 2. Responsible for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information, based on information from all relevant line functions, postmarketing data, and other sources. 3. Develops and updates, at milestones, the safety profiling and risk management plan from end of Phase I (POC) through Life Cycle Management, as relevant. 4. Leads Safety Management Team. Serves as safety representative on Global Program Teams (extended or core member) 5. Manages Drug Safety Monitoring Board activities for assigned projects/products, as required. 6. Responsible for responses to inquires from regulatory authorities or health care professionals on safety issues. Prepares safety data for health authority review boards. Responsible for responses to legal queries andCPO requests involving safety issues. Ensures safety informa-tion communicated to EU Qualified Person in a timely fashion. 7.Provides integrated safety input into all safety relevant parts of regulatory documents (ie IB, CDS, SCS, RMP, CO etc) requiredduring active development, submission phase and during marketing phase. 8. Co-ordinates involvement of external experts (e.g.authors of "white papers", members of trial-specific data safety monitoring boards, ad-hoc support for HA meetings, etc.# 9. Prepares and may present project/product safety issues to internal Boards, or expert panels and other meetings 10. Collaborates productively with colleagues from Clinical Research, Drug Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments. 11. Provides support as needed for licensing activities, regulatory authority inspections and for project/product recall activities. 12. Serves as and performs activities of Pharmacovigilance Leader as needed. Minimum requirements : o Medical Degree absolutely required. Specialty Board certificate desirable. o Languages: English. Understanding in another major language #e.g. French, German, Spanish# desirable. o 3 years medical experience postdoctoral o At least 5 years in industry or health authority or CRO #of which 2 years in a global position#, in-cluding a minimum of 3 years in drug safety o Experience in preparing clinical safety assessments, risk/benefit evaluations and regulatory re-ports o Experience in leading cross-functional, multi-cultural teams o Experience in preparing RMPs, PSURs, Submission dossiers #SCS#. Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: RMPs, PSURs, Submission dossiers (SCS). Job Reference: KP1007-27 http://www.hallolondon.co.uk/index.html?op=3&id=519996 Job duration: Permanent Start date: ASAP Description: Our global client in Central France is looking for a Brand Safety Leader to join their team on a permanent basis. Job Description : Serves as scientific safety leader for assigned projects/products . Once the project team is formed, responsible for the integration, analysis, and interpretation of safety information from all sources, including preclinical through lifecycle management (postapproval) and externally. 1. Responsible for safetyissue management from end of Phase I (POC) through Life Cycle Man-agement. 2. Responsible for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information, based on information from all relevant line functions, postmarketing data, and other sources. 3. Develops and updates, at milestones, the safety profiling and risk management plan from end of Phase I (POC) through Life Cycle Management, as relevant. 4. Leads Safety Management Team. Serves as safetyrepresentative on Global Program Teams (extended or core member) 5. Manages Drug Safety Monitoring Board activities for assigned projects/products, as required. 6. Responsible for responses to inquires from regulatory authorities or health care professionals on safety issues. Prepares safety data for health authority review boards. Responsible for responses to legal queries andCPO requests involving safety issues. Ensures safety informa-tion communicated to EU Qualified Person in a timely fashion. 7. Provides integrated safety input into all safety relevant parts of regulatory documents (ie IB, CDS, SCS, RMP, CO etc) required during active development, submission phase and during marketing phase. 8. Co-ordinates involvement of external experts (e.g. authors of "white papers", members of trial-specific data safety monitoring boards, ad-hoc support for HA meetings, etc.# 9. Prepares and may present project/product safety issues to internal Boards, or expert panels and other meetings 10. Collaborates productively with colleagues from Clinical Research, Drug Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments. 11. Provides support as needed for licensing activities, regulatory authority inspections and for project/product recall activities. 12. Serves as and performs activities of Pharmacovigilance Leader as needed. Minimum requirements : o Medical Degree absolutely required. Specialty Board certificate desirable.o Languages: English. Understanding in another major language #e.g. French, German, Spanish# desirable. o 3 years medical experience postdoctoral o At least 5 years in industry or health authority or CRO #of which 2 years in a global position#, in-cluding a minimum of 3 years in drug safety o Experience in preparing clinical safety assessments, risk/benefit evaluations and regulatory re-ports o Experience in leading cross-functional, multi-cultural teams o Experience in preparing RMPs, PSURs, Submission dossiers #SCS#. Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Medical Degree, Oncology, Post doctoral, PSURS, RMP Job Reference: KP1007-25 http://www.hallolondon.co.uk/index.html?op=3&id=519990 Job duration: Permanent Start date: ASAP Description: Our client looking for a Clinical Feasibility Specialist II to join their teams on a permanent based in both Middlesex, UK and Germany. Essential Function Provide feasibility assessments for new business opportunities or awarded studies including supervision of external investigator surveys and coordination of other support groups as required. Develop operational strategies including scenario planning (country/site optimization) and support the preparation of bid defense meetings. Provide expertise in the recruitment and selection of qualified investigators in support of clinical projects by data mining internal data assets and using external data if appropriate. Working in close collaboration withlocal Clinical Trial Specialists staff in various countries. Contribute to strategies to improve the customer relationship withsites, including development of new models of collaboration. Analyze and work to continuously improve predictive investigator performance metrics. Key Accountabilities �Assume the ability to meet the requirements of a CFS I with a high degree ofproficiency and autonomy �Perform feasibility assessment of clinical protocols to assess the operational impact by theprotocol design, interpretation of past performance data and it�s relevance to the current protocol, coordinate the inputfrom other expert groups (Medical Services, Study Start-Up, Regulatory Affairs and Patient Recruitment Strategy Group) into thefeasibility assessment that is being delivered to the proposal writer �Develop recommendations for country allocation and site distribution inclusive of scenario planning by using the SPARC application �Develop feasibility and site selection slides with the support of Clinical Feasibility Specialist I in case of external survey for presentation at the bid defense meeting �Support the development of the proposals and costing for stand-alone Feasibility & Clinical Informatics services including proposal revisions as needed and contract review �Provide work instructions and guidance to Clinical Feasibility Specialist I & II and Clinical Informatics Specialists I & II for the conduct of questionnaire-based investigator surveys. �Perform quality review of feasibility/pre-qualification questionnaires and related reports/slides presentingthe survey results. �Prepare site lists by using data mining of internal and external data assets, using investigator performance data �Develop and support the implementation of site selection strategies in support of clinical projects in close collaboration with Clinical Trial Specialists in various countries and project teams. �Develop and implement strategies for improving investigator relationship management including new ways to collaborate with investigators, SMOs and otherinvestigator organisations. �Analyze and work to continuously improve predictive investigator performance metrics in support of site selection. �Assist in the development of programs to recruit and maintain a qualified pool of investigatorsin support of projects in all therapeutic areas. �Attend client meetings on an ad hoc basis �Keep manager informed about work progress and any issues to avoid surprises. Requires some interaction / supervision by Manager or assigned mentorSkills �Sense of urgency, initiative, and diplomacy �Strong analysis and synthesis skills �Working knowledge of worldwide clinical research �Sound interpersonal, verbal and written communication skills �Ability to manage multiple tasks with enthusiasm and prioritise workload with attention to detail Education �Educated to a degree in Science, possibly in Life Sciences, or relevant qualification/experience �Significant experience in clinical research within a CRO including appropriate expertise in feasibility assessments and/or clinical monitoring study coordination and/or site and investigator relationships Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Clinical, Feasibility Job Reference: KP1004-76 http://www.hallolondon.co.uk/index.html?op=3&id=519607 Job duration: 5 months Start date: 26/07/2010 Description: Contract European Medical Information Specialist Position Purpose: European Medical Information is a customer-focused group within External Medical Communications that is responsible for responding to unsolicited inquiries regarding human prescription products and devices. Primary Duties: - Exhibits broad knowledge of assigned therapeutic area and a solid understanding of pertinent disease state(s) - Handles escalated MI inquiries from various sources - intensive medical writing - Analyzes inquiry data to identify trends and communicates salient pointsto the Product/Therapeutic Team(s) and to in-Countries Medical Directors and/or local Business Units - Act as Regional MedicalInformation contact point for local issues and medical communications - Creates and maintains European MI documents by ensuring that responses are medically and scientifically accurate, timely, fair balanced and meet customers' needs. Ensures the alignment of response documents to European/local labelling and licensing for all the Countries we serve - Proactively seeks continuous improvement in MI processes and responses - Together with the Brand and Medical Teams, facilitates the development and maintenance of formulary-related documents in support of improving access to managed care formularies and their distribution through the call centers - Represents the Company by providing live MI support at scientific conventions/congresses; may serve as the lead for coordinating the MI function at scientific conventions/congresses - Maintains compliance with corporate and departmental trainings, standard operating procedures, and implementation guidelines - Provides an MI perspective on the development andrevision of standard operating procedures and implementation guides as necessary Qualifications and Experience: - Candidates with pertinent industry-related experience and/or post-graduate specialty/residency are desirable - PharmD, BS in Pharmacyor MD/DO strongly preferred. Degrees from other medical disciplines and non medical candidates with previous relevant experiencealso considered. Multilingual candidates are also highly sought after. - One to three years of medical information experiencepreferred - Demonstrates effective relationship management and customer orientation - Demonstrates strong oral and written communication skills - Able to work in a fast-paced environment with competing priorities If you meet the above requirements and you are looking for a new opportunity, please call Cherise or send your CV with a short cover note highlighting your relevantexperience. SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £1per hour Job type: Contract Job skills: medical information Job Reference: CQPMIS http://www.hallolondon.co.uk/index.html?op=3&id=517963 Job duration: Start date: ASAP Description: Our Clientis an independent upstream oil and gas company headquartered in Calgary, Alberta, Canada. The main business activities include exploration, development, production, transportation and marketing of crude oil, natural gas, and natural gas liquids (NGLs). The company has operations in Canada, and its subsidiaries operate in the UK, Norway, Southeast Asia, South America, NorthAfrica and the US and are also active in other international areas. They currently now have an outstanding opportunity for aReservoir Engineer based in Aberdeen. Reporting to the Team Lead, Exploration, the successful candidate will be responsiblefor conducting analytical and empirical reservoir studies for producing and pre-development reservoirs, complemented by exposureto the G&G and Drilling/Completions disciplines. In this position you will work closely with Geophysical & Geological team on input data for studies and provide support to exploration program. This role will be responsible for: * Maintain and update reservoir engineering database inclusive of daily production data, core and fluid analysis, pressure surveys / PBUs. * Perform daily well and reservoir surveillance for Phase I production wells. * Develop and run reservoir simulation modelsfor PNG oil and gas fields. * Conduct analytical and empirical reservoir studies for producing and pre-development reservoirs.* Develop and monitor Reservoir Management plan & Reservoir Depletion strategy. * Conduct Field Development Planning exercise to optimize well locations, well utilities and well counts * Evaluate enhanced oil production opportunities and diagnostics/mitigation of abnormal well behaviours. * Make production forecasts for planning exercises and economic evaluations. * Execute regular reporting exercises such as Quarterly Capacity review, monthly production reports, reserves reporting and adhoc requests by Partners. * Provide support to Operations, Projects and Drilling Departments and liaise with Partners/contractors/vendors. Skills required for Reservoir Engineer * B.Sc /B.A. or higher degree in Petroleum Engineering combined with 7-10 years ofexperience * Proficient in reservoir simulation (Eclipse). * Reservoir performance and forecasting expertise. * Reservoir fluid and rock assessment. * Fluid typing and basic processing requirements. * Well logging and log interpretation. * Proficient in wide range of reservoir simulation software packages. * Experienced in full range of basic engineering criteria, includinglogging, PVT and core analysis. * Communication of complex engineering concepts. Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Reservoir Job Reference: 00052 http://www.hallolondon.co.uk/index.html?op=3&id=517630 Job duration: Permanent Start date: August 2010 Description: Our client in Surrey is looking for a Surveillance Associate/Scientist to jointheir expanding team on a permanent basis. The purpose of the Surveillance Associate / Scientist is to perform safety surveillance of products through signal detection and clarification, preparation of periodic and ad-hoc safety reports, effective analysis and communication of safety related questions to internal and external customers, and to promote and advance the field ofGlobal Patient Safety. Key Responsibilities: 1. Signal Detection/Clarification o Effectively utilize available tools toidentify, clarify and communicate potential safety signals from multiple data sources. o Consult and coordinate with safety physicians and other appropriate personnel to ensure thorough evaluation of safety signals. o Effectively communicate relevantsafety information to the appropriate persons. o Actively participate in therapeutic area and departmental safety meetings.2. Safety Inquiries o Define evaluation plan with partners (physicians, team members, business partners) to appropriately assess and complete responses for inquiries from both regulatory authorities and other internal and external sources regarding product safety. 3. Periodic Reports/ Pharmacovigilance (PV) Plans o Complete the analysis of the safety data related sections and maintain oversight of periodic reports such as Periodic Safety Update Reports (PSURs), Periodic Adverse Drug Experience Reports (PADERs), European Union (EU) Annual Safety Reports and Ethical Review Board (ERB) Line Listing Reports. o Meet periodic reporting requirements as per the periodic reports calendar. o Prepare and maintain PV plans. o Identify and propose process improvements. 4. Promote and advance the field of Global Patient Safety o Develop critical relationships with internal customers (e.g. product teams, regulatory, GOLD). o Develop expertise in surveillance activities and documents and apply shared learning and influence across the surveillance team. o Ensure quality and compliance is maintained. o Conduct safety surveillancetraining (external and internal). o Understand the roles and responsibilities of the EU Qualified Person. Job Requirements: o Education: Bachelors degree or higher in the healthcare field (with preference given to pharmacy, medical or nursing)or equivalent demonstrated clinical experience o Experience within Global Patient Safety or demonstrated understanding of Pharmacovigilance and Pharmacoepidemiology o Clinical knowledge of various disease states, human physiology and pharmacology oStrong Analytical/Quantitative Skills o Effective communication skills to interact with diverse groups and individuals o Demonstrated consistent delivery of high quality on time work products Other Information: Preferred Skills: o Knowledgeof global safety regulations o Ability to manage multiple tasks simultaneously Industry: Science and Research Salary currency: gbp Salary Benefits: benefits Salary: £35000 - £42000 per annum + benefits Job type: Permanent Job skills: PSURS, European Drug Safety Job Reference: KP1006-88 http://www.hallolondon.co.uk/index.html?op=3&id=514526 Job duration: 6 months Start date: asap Description: For my client, an international pharma, a leaderon the market, I am currently looking for a Process Engineer to work on a 6 month contract with a possibility of extension. Asuitable candidate will be responsible for overseeing the technical performance and compliance of the drug production processes.Applicants should have the knowledge and experience of manufacturing process operations gained in a pharmaceutical or food processing environment. In order to be successful they will also need to have experience in data management and statistical analysis . Great communication skills, ability in problem solving together with a degree in scientific or engineering discipline and aproven ability to understand and analyse process data are also required from the candidates. My client offers a 6 month contract, an opportunity to join a leading pharmaceutical company, competitive hourly rate and a possibility of the contract extension.For an immediate application and a full job description please forward your CV to agata.lugowska@secpharma.com or call our office on (0) 2072556600 Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £20 - £22 per hour Job type: Contract Job skills: engineer, pharmaceutical Job Reference: 009123 http://www.hallolondon.co.uk/index.html?op=3&id=513798 Job duration: 6 months Start date: asap Description: For my client, an international pharma, a leaderon the market, I am currently looking for a Process Engineer to work on a 6 month contract with a possibility of extension. Asuitable candidate will be responsible for overseeing the technical performance and compliance of the drug production processes.Applicants should have the knowledge and experience of manufacturing process operations gained in a pharmaceutical or food processing environment. In order to be successful they will also need to have experience in data management and statistical analysis . Great communication skills, ability in problem solving together with a degree in scientific or engineering discipline and aproven ability to understand and analyse process data are also required from the candidates. My client offers a 6 month contract, an opportunity to join a leading pharmaceutical company, competitive hourly rate and a possibility of the contract extension.For an immediate application and a full job description please forward your CV to agata.lugowska@secpharma.com or call our office on (0) 2072556600 Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £20 - £22 per hour Job type: Contract Job skills: engineer, pharmaceutical Job Reference: 009123 http://www.hallolondon.co.uk/index.html?op=3&id=511185 Job duration: Permanent Start date: ASAP Description: Our client looking for a Clinical Feasibility Specialist II to join their teams on apermanent based in both Middlesex, UK and Germany. Essential Function Provide feasibility assessments for new business opportunities or awarded studies including supervision of external investigator surveys and coordination of other support groups asrequired. Develop operational strategies including scenario planning (country/site optimization) and support the preparation ofbid defense meetings. Provide expertise in the recruitment and selection of qualified investigators in support of clinical projects by data mining internal data assets and using external data if appropriate. Working in close collaboration with local Clinical Trial Specialists staff in various countries. Contribute to strategies to improve the customer relationship with sites, including development of new models of collaboration. Analyze and work to continuously improve predictive investigator performance metrics. Key Accountabilities �Assume the ability to meet the requirements of a CFS I with a high degree of proficiency and autonomy �Perform feasibility assessment of clinical protocols to assess the operational impact by the protocoldesign, interpretation of past performance data and it�s relevance to the current protocol, coordinate the input from other expert groups (Medical Services, Study Start-Up, Regulatory Affairs and Patient Recruitment Strategy Group) into the feasibility assessment that is being delivered to the proposal writer �Develop recommendations for country allocation and sitedistribution inclusive of scenario planning by using the SPARC application �Develop feasibility and site selection slides with the support of Clinical Feasibility Specialist I in case of external survey for presentation at the bid defense meeting�Support the development of the proposals and costing for stand-alone Feasibility & Clinical Informatics services including proposal revisions as needed and contract review �Provide work instructions and guidance to Clinical FeasibilitySpecialist I & II and Clinical Informatics Specialists I & II for the conduct of questionnaire-based investigator surveys. �Perform quality review of feasibility/pre-qualification questionnaires and related reports/slides presenting the survey results. �Prepare site lists by using data mining of internal and external data assets, using investigator performance data �Develop and support the implementation of site selection strategies in support of clinical projects in closecollaboration with Clinical Trial Specialists in various countries and project teams. �Develop and implement strategiesfor improving investigator relationship management including new ways to collaborate with investigators, SMOs and other investigator organisations. �Analyze and work to continuously improve predictive investigator performance metrics in support ofsite selection. �Assist in the development of programs to recruit and maintain a qualified pool of investigators in support of projects in all therapeutic areas. �Attend client meetings on an ad hoc basis �Keep manager informed about work progress and any issues to avoid surprises. Requires some interaction / supervision by Manager or assigned mentor Skills �Sense of urgency, initiative, and diplomacy �Strong analysis and synthesis skills �Working knowledgeof worldwide clinical research �Sound interpersonal, verbal and written communication skills �Ability to managemultiple tasks with enthusiasm and prioritise workload with attention to detail Education �Educated to a degree inScience, possibly in Life Sciences, or relevant qualification/experience �Significant experience in clinical research within a CRO including appropriate expertise in feasibility assessments and/or clinical monitoring study coordination and/or siteand investigator relationships Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Clinical,Feasibility Job Reference: KP1004-76 http://www.hallolondon.co.uk/index.html?op=3&id=509624 Job duration: Permanent Start date: ASAP Description: An opportunity has arisen for a Senior Scientist to join my client based in the Buckinghamshire area on a permanent basis. Description The successful candidate will be responsible for the production ofPSURs, FDA NDA Periodic Reports, and FDA IND Annual Reports for assigned therapeutic areas. This will include the followingactivities: managing the production of timely, quality aggregate reports for assigned products, including planning and liaison with Global Medical Safety physicians and other groups to guide report content, report writing (summarising information on individual cases in aggregate), analysis to assess adequacy of current reference safety information, data quality review/correction, evaluating and addressing comments from reviewers of draft reports for appropriateness, and assembly in a document management system. Responsibilities also include management of therapeutic area issues/workload with colleagues and the support of the Manager; coaching/mentoring newer team members; evaluating the input of other team members/functional areas in this process; quality review of team members' work; participation in cross-functional, intra- and inter-departmental teams or assignments as required; interpreting and addressing Regulatory Assessor comments; and (re)prioritisation of work to manage projects. Skills The successful candidate will have good interpersonal skills and mentoring skills. They will be detail oriented, and have project management skills. They should be an independent worker who is also able to participate as a team member. The candidate willdemonstrate strong CREDO values. The successful candidate will have excellent verbal and written communication skills, plusgood computer skills including competence with Microsoft Word (tables and basic formatting), competence with Microsoft Excel andweb-based program/internet and familiarity with Documentum systems, Windows OS. Experience/Qualifications Bachelor's Degree (or higher preferred) in Health/Biomedical Sciences or equivalent degree. Experience in aggregate report writing (samplesand extemporaneous may be requested) is required, also in drug safety (e.g. single case processing; familiarity with safety database systems). Candidates should be familiar with global safety regulatory requirements and with safety resources. Experience is typically gained from a minimum of 3 years in drug safety. Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Experience in aggregate report writing Job Reference: KP1002-104 http://www.hallolondon.co.uk/index.html?op=3&id=509513 Job duration: Permanent Start date: ASAP Description: Technical Lead - Waste Radiochemistry, Measurement and Analysis Lancashire Attractive salary package Role Description Supervise and technically direct laboratory staff for a core technical team that provideswaste radiochemistry, analytical, and measurement and testing services to nuclear facility operators. Duties Technically directing a portfolio of work for the Analysis and Testing Laboratories to UKAS Accreditation standards. Responsible for all aspects of the sample life cycle e.g. organising the receipt, unpacking, processing, analysis, and return or disposal of samples.Planning and organising the workload of the team on a day-to-day basis. Responsible for successful completion of signed up work programmes to agreed technical scope within established time, cost and safety standards. Assist the Technical Manager and Technical Team Leader in identifying development needs for the team and implementing personal development plans. Provide technical input and hours estimates into bids and proposals. Comply will legislative, regulatory and company policy, standards and procedures applicable to the role. Assist the Team Manager in maintaining appropriate UKAS standards, systems and documentation.Essential Skills and Qualifications Radiochemisrty experience Experience of working in a busy UKAS Accredited ChemistryLaboratory. BSc/Degree level Chemistry or equivalent qualification. Experience of checking and verifying technical work prior to customer release. Experience of provision of technical scope and hours estimates into bids/proposals. Desirable Skills and Qualifications Experience of preparing method statements / work instructions and method development. Experience or knowledge of a Quality Manager role. Experience of sample management. Previous role in consumables ordering and management ofconsumables budget. Working knowledge of technical equipment such as gamma/alpha spectrometry, LSC. Experience of managingsafety of laboratory operations To apply contact Joseph Ghayour at Intec Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £35000 - £60000 per annum Job type: Permanent Job skills: Job Reference: JG9987 http://www.hallolondon.co.uk/index.html?op=3&id=504040 Job duration: perm Start date: asap Description: For my client, an established Clinical Research Organisation expanding their operations in Europe I am currently looking for an experienced Clinical Research Associate to join their hugely successful team. On this position you will be mainly responsible for: * Clinical monitoring * Investigators' recruitment* Maintaining contact with Investigators and sites * Negotiate study budgets * Train and mentor more junior CRAs * Assist in preparation and maintenance of clinical trials' documentation A detailed job description will be provided upon application.Applicants should posses a life science degree, be experienced Clinical Research Associates, have exposure to oncology or neurology trials, have excellent verbal and written communication skills. In return my client offers a competitive salary of up to38 000 GBP combined with an annual bonus and a car allowance , an exceptional benefits package including pension scheme, medicalinsurance and 25 days of holiday among others. For an immediate consideration please forward your CV to agata.lugowska@secpharma.com or call Agata on 0044(0)2072556600 Industry: Science and Research Salary currency: gbp Salary Benefits: negotiable, benefits Salary: £35000 - £38000per annum + negotiable, benefits Job type: Permanent Job skills: clinical, CRA, monitoring Job Reference: 9379 http://www.hallolondon.co.uk/index.html?op=3&id=503983 Job duration: 6 months Start date: asap Description: For my client, one of the biggest and most prestigious pharmaceutical companies in the world I am currently looking for a Laboratory Technician with the sound knowledge of microbiological testing. On this 6 month contract role you will be mainly responsible for: * testing products, materials and generating laboratory results against the agreed Quality Standards to ensure the quality, safety and efficacy of these products to the customer or user. * ensuring the appropriate quality systems are followed in order for the laboratory to meet its responsibilities with respect to GCLP,GMP and SHE.* using knowledge of LEAN tools and techniques to demonstrate continuous improvement and perform appropriate tasks in the laboratory to meet customer demand. An ideal candidate will be an experienced Laboratory Technician with experience in microbiological testing, be qualified to A level in Chemistry or Biology, be located in Cheshire area and be available to start on asap basis. In return my client offers a 6 month contract with a possibility of extension, an hourly rate of £10 and an opportunity towork for one of the most prestigious pharmaceutical companies in the world. For a detailed job description, more information about this opening and for an immediate consideration please send your updated CV with a short cover letter describing your current situation to agata.lugowska@secpharma.com . You can always contact Agata on (0) 2072556600 for a confidential conversation. Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £10 per hour Job type: Contract Job skills: laboratory Job Reference: 0884 http://www.hallolondon.co.uk/index.html?op=3&id=503912