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: 6months+ Start date: ASAP Description: 6 month rolling contract Job Summary: The Statistical Project Programmer performs the planning and implementation of resource allocation and leads the statistical programming activities such that agreed objectives, standards, deadlines and other requirements with respect to specifications, development, quality assurance and delivery areattained in accordance with applicable processes. Accountabilities/Responsibilities: * Lead the statistical programming activities on a project. Provide direction and focus on programming activities related to analysis and reporting of results onthe assigned drug development project. * Provide expert knowledge to Biostatistics on statistical programming strategies. Assess and clarify requirements, provide statistical programming solutions and ensure their effective implementation. * Oversee the programming specifications within the project and ensures consistency with the statistical requirements for analysis datasets(VADs), pooled datasets, listings, tables, and figures. Assist as appropriate. Essential Skills & Capabilities: * University education or equivalent in Mathematics, Statistics, Computer Science or other analytical field. * At least 8-10 years ofpharmaceutical industry drug development experience using SAS. * Expert knowledge of SAS programming language, with SAS/Base,SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS. * Good knowledge of drug development process in particular on collection, storing, processing and analysis of clinical trial data. * Good knowledge of English, communicating clearly and effectively inwritten and oral form in a business environment. * Well developed planning , organizational and analytic abilities * Stronginterest in establishing and maintaining a respectful and effective working environment. For further details or a confidential conversation please contact me directly: James Carrera Manager - Pharmaceutical, Healthcare & CRO Division Statistics, Biostatistics & Programming Tel: +44 (0) 207 255 6665 james.carrera@secpharma.com http://uk.linkedin.com/in/jamescarrera Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £50 per hour Job type: Contract Job skills: Job Reference: 0902/12b http://www.hallolondon.co.uk/index.html?op=3&id=791541 Job duration: perm Start date: negotiable Description: A brand new permanent opportunity for an In-House CRA-remote monitoring-minimal travel-office based in West London-Leading CRO! For my client, a prestigious international fast-growing Clinical Research Organisation I am now looking for an experienced Clinical Research Associate who would join my client's international team. The responsibility of a Clinical Monitoring Associate is to perform remote clinical monitoring tasks and remote visits for designated projects in accordance with relevant SOPs, study specific procedures and regulations. Responsibilities include managing, coordinating and supporting of clinical monitoring activities remotely, including issue resolution, patient enrolment management, handling protocol and ensuring timely data entry at a site level. A successful candidate for this position will be educated to degree level ideally in life sciences, will have previous clinical monitoring experience on a CRA or an In-House CRA position. They will have very good command of English and will be prepared to work office-based in my client's West London's office. This is an amazing opportunity for an experienced CRA who would like to limit their travels and who is aiming at creating a better work/life balance. Stable permanent role would suit an established professional whois looking to for a secure employment and constant flow of new projects. Ambitious and driven individuals can count on an opportunity to progress within this international organisation! Rewarding basic salary combined with numerous benefits are waiting for the successful candidate! For an immediate consideration please forward your cv to agata.lugowska@secpharma.com or contact me on (0) 2072 55 66 65 for a confidential discussion about your next career move Industry: Science and Research Salary currency: gbp Salary Benefits: negotiable+benefits Salary: £26000 - £35000 per annum + negotiable+benefits Job type: Permanent Job skills: clinical, monitoring, cra, London Job Reference: 140990 http://www.hallolondon.co.uk/index.html?op=3&id=790565 Job duration: Start date: ASAP Description: Analytical Development Chemist My Client, a world leading pharmaceutical company, is looking for a talented individual to work as Analytical Development Chemist. The professional we are looking for has to be fluent in German andEnglish. You will lead the analytical development team, working on new analytical methods and validate them according to GMPguidelines and ICH guidelines. You will also carry out the characterization of the iron compounds. In addition to testing new primary packaging materials, the job will include indicative stability measurements and the evaluation of new analytical techniques. The right candidate is a chemist with a focus on analytical chemistry and have good knowledge of instrumental analysis (LC-MS, ICP-MS, ICP-OES) and experience in the use of biochemical methods such as ELISA and gel electrophoresis (eg. SDS-PAGE).My Client can offer an exciting and interesting opportunity for individual initiative and career development in a growing company with a great working environment. To apply, forward your CV to Sergio.carito@secpharma.com Call Sergio Carito on + 44(0)207 255 66 65 for further information and a confidential discussion of this opportunity. SEC Recruitment Limited is acting asan Employment Agency and/or Employment Business Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Job Reference: 7744465 http://www.hallolondon.co.uk/index.html?op=3&id=788394 Job duration: Start date: asap Description: My Client, a world leading pharmaceutical company, is looking for a talented individual to work as Pre-Clinical Research Scientist. The professional we are looking for has to be fluent in German and English. Acting as study director and study personnel for non-clinical studies (GLP-studies according to GLPV SR 813.112.1 and non-GLP-studies), You will create study protocols and reports for GLP- and non-GLP-studies, according to GLP-Guidelines. You will perform animal studies supporting the implementation of new in vivo (disease) models. You will also cooperate with department for chemical research and development for test item delivery, formulation and application and with Biology Group for conduction of animal?s studies and provision of test material. Other important responsibilities are the cooperation with QA-department for GLP-compliance and the support to internal audits. With a Degree in life sciences, pharmacology or veterinary pathology and training for conducting animalexperiments (LTK-Module 1 or 2), the right candidate is experienced to work with rodents (drug application techniques, samplingof specimens like blood, organs or cells) and with different animal models (inflammation, oncology, nephrology would be an asset). This role requires experience with different analytical methods, preferably haematological, biochemical and immunological methods (FACS analysis, histology) and in-depth knowledge of appropriate statistical methods for data analysis, GLP regulation.My Client can offer an interesting and challenging function in a young, motivated team as well as the advantages of a modern company with excellent social benefits. To apply, forward your CV to Sergio.carito@secpharma.com Call Sergio Carito on + 44(0)207 255 66 65 for further information and a confidential discussion of this opportunity. SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: Job type: Permanent Job skills: Job Reference: 717661 http://www.hallolondon.co.uk/index.html?op=3&id=788393 Job duration: 6 Months Start date: asap Description: A new freelance project has justbecome available for an experienced Clinical Research Associate in one of the most prestigious Clinical Research Organisations in the world! This is a 6-month freelance contract for an experienced Clinical Research Associate to monitor clinical sites located in the Republic of Ireland working in a full time capacity. This freelance opportunity would suit an experienced Clinical Research Associate looking for a new project and it would be ideal for a professional with extensive experience in Neurology. A CRA wishing to apply for the role will need to be located within a commutable distance from Dublin area, they will be available to start freelancing with a short notice and they will have full time availability to devote to the client. A successful candidate will be rewarded will an excellent daily rate, an opportunity to work on 6 month contract, possibility of the contract extension, great working atmosphere and one of a kind opportunity to gain experience in an international Clinical Research Organisation. For an immediate consideration please forward your CV to agata.lugowska@secpharma.com or contact our office on (0) 2072 5566 65 Industry: Science and Research Salary currency: gbp Salary Benefits: negotiable Salary: negotiable Job type: Contract Job skills: clinical, monitoring, CRA, Ireland, Irish Job Reference: 150009 http://www.hallolondon.co.uk/index.html?op=3&id=787791 Job duration: 6 mths Start date: 28/02/2012 Description: Our global client is looking for a Diabetes Scientific Advisor to join their team on a 6 months contract. Work with the diabetes team in making launch preparationsfor a product, including: overseeing and participating in the preparation of standard Medical Information letters; working closely with the Medical Information Officers to answer complex enquiries; keeping up-to-date with recent therapy and competitor newsand advising the brand team accordingly; helping shape the generation of marketing campaigns by providing scientific expertiseto the brand team; copy approval of promotional material to ensure compliance with the ABPI Code of practice. Requirements: at least 2 years experience (including Medical Information); experience of copy approval (preferably using Zinc), producing standard letters; proficiency in literature searching; good standard of written English; experience of working in the diabetes therapy area. Industry: Science and Research Salary currency: gbp Salary Benefits: upon application Salary: upon application Job type: Contract Job skills: "Scientific Adviser" "Diabetes" "Zinc" "ABPI Code of Practice" Job Reference: KP1202-6 http://www.hallolondon.co.uk/index.html?op=3&id=787384 Job duration: 6 months Start date: ASAP Description: For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@secpharma.com IMMEDIATE BUSINESS NEED Excellent Rate - £50-55 / hour 6 month+, Immediate Start Available & preferred, but they will wait for notice Based in SouthEast, UK This position is 100% office-based due to the nature of the work Accountabilities/Responsibilities: - Lead thestatistical programming activities on a project. Provide direction and focus on programming activities related to analysis and reporting of results on the assigned drug development project. - Provide expert knowledge on statistical programming strategies.Assess and clarify requirements, provide statistical programming solutions and ensure their effective implementation. - Guidestatistical programming team members on trial protocol review, CRF development and data structure specifications for clinical trials. Ensure consistency and adherence to available standards. - Oversee the programming specifications within the project andensures consistency with the statistical requirements for analysis datasets, pooled datasets, listings, tables, and figures. Assist as appropriate. - Lead activities on programming, validation and documentation according to the agreed specification, pooled datasets, listings, tables, and figures. Ensure that high quality standards, consistency within the project and delivery within agreed time lines are being met. Assist as appropriate. - Ensure adherence to statistical programming standards, effective use of available standard programs, availability of appropriate documentation and compliance with Standard Operating Procedures.- Act as PoC, liaising with sponsors, customers and other functional areas as required. Essential Skills & Capabilities:- At least 6 years of pharmaceutical industry drug development experience using SAS. - Expert knowledge of SAS programminglanguage, with SAS/Base, SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS. - Good knowledge of drug development process in particular on collection, storing, processing and analysis of clinical trial data. - Good knowledge of English, communicating clearly and effectively in written and oral form in a business environment. - Well developed planning , organizational and analytic abilities - Strong customer focus For a confidential consultation call; James Carrera Statistics, Biostatistics & SAS Programming Pharmaceutical Division Tel: +44 (0)20 7255 6600 Fax: +44 (0)20 7255 6656 Email: James.Carrera@secpharma.com Web: www.secrecruitment.com 3rd Floor, Woolverstone House, 61-62 Berners Street London W1T 3NJ United Kingdom SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £50 - £55 per hour Job type: Contract Job skills: sas statistical programmer base macro clinical pharma pharmaceutical Job Reference: 131/12b http://www.hallolondon.co.uk/index.html?op=3&id=780682 Job duration: Start date: Description: Clinical Research Organisation-Buckinghamshire area-Site Management Team Leader-up to 30 000 GBP+ numerous benefits-immediate start! With a Fantastic New Year ahead we are now introducing a brand new opportunity that has just become availablewithin a leading international Clinical Research Organisation located in Buckinghamshire area in a position as a Site ManagementTeam Leader. The candidates suitable for such role must demonstrate strong knowledge of clinical administration and EC andRegulatory submissions processes. They will also be able to prove their leadership and management experience and strong communication and leadership skills. The location of this role is in Berkshire/ Buckinghamshire so candidates will need to consider thecommute and be in close proximity of these areas. A successful candidate will be rewarded with a permanent role in a fast growing yet well-established international company and an opportunity to grow within this well-recognised organisation. They willbe offered a basic salary of up to 30 000 GBP per Annam with additional benefits. For immediate consideration and a full jobdescription please forward your CV to Bradley.doyle@secpharma.com or call + 44 (0) 207 255 6665 Keywords: Clinical administrator, line manager, Clinical trial administrator, Clinical trials associate, Administrator, Manager, Diabetes, Obesity, Pain, CNS, HIV, Oncology, Cardiovascular, Respiratory, Therapeutic, Development, Career, Progression, job, role, Study Management, SiteManagement, CRO, Pharmaceutical, Clinical Operations Industry: Science and Research Salary currency: gbp Salary Benefits: Benifits Salary: £29000 - £30000 per annum + Benifits Job type: Permanent Job skills: Clinical administrator, line manager, Clinical trial administrator, Clinical trials associate, Administrator, Manager, Diabetes, Obesity, Pain,CNS, HIV, Oncology, Cardiovascular, Respiratory, Therapeutic, Development, Career, Progression, job, role, Job Reference: 030391 http://www.hallolondon.co.uk/index.html?op=3&id=779593 Job duration: Start date: ASAP Description: My Client, Global Multinational Company headquartered in Italy, is seeking a target oriented, self-motivated individual who would be interested in working as Analytical Senior Scientist on a permanent basis. Key Responsibilities: -Development and Validation of Drug Substance (DS) & Drug Product (DP) analytical method; -Transfer the analytical methods toR&D QC; -Identify the Critical Quality Attributes for both Drug Substance and Drug Product (including interaction with device and CCS), for the appropriate definition of critical specifications and related scientific justification; -Ensure that DS/DP characterization is conducted in accordance to Company SOPs and protocols and with cGMP/ICH where applicable; -Ensure that all laboratory documentation is completed according to company standards including all relevant investigations; -Ensure a continuous innovation of the analytical technologies, in order to keep a high level and excellence of scientific know-how. -Develop scientific networking, interacting with advanced CROs/academia. With a Ph.D. in Analytical Techniques and at least six years of relevant pharmaceutical & analytical development experience in a well-structured company, the ideal candidate has got an international experience, strong knowledge of modern analytical techniques and development of different pharmaceutical forms, good understanding of analytical method development & validation requirements of pharmaceutical industry, a good knowledge of chromatographic sciences and spectroscopic technologies e.g. UV, IR, MS, NMR, XRD. Strong knowledge of characterization techniques in physical and aerodynamic properties, chemical and solid state stability. The right candidate is a scientific problem solverwho works well independently and in a team environment and with the determination and ability to foster organisational and cultural (i.e. scientific and innovation) change. Strong knowledge about Drug Substance/Excipients compatibility studies and good understanding of cGMP, ICH and FDA requirements. Additional experience in pharmaceutical dosage forms for pulmonary delivery [i.e.Pressurized Metered Dose Inhalers (pMDI's), dry powder inhalers (DPI), liquid-nebulizers (UDV)] could be relevant. Fluent in English, good communication skills are required. My Client offers a permanent position, competitive salary and generous social benefits, the opportunity for development and advancement within a constantly growing company and an innovative and stimulating atmosphere of a multicultural environment, plus a relocation package. If you are interested in this new, exclusive career opportunity, please email your application to sergio.carito@secpharma.com or call Sergio Carito on +44 207 255 6665. SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: €40000 - €50000 per annum Job type: Permanent Job skills: Job Reference: 706662 http://www.hallolondon.co.uk/index.html?op=3&id=778849 Job duration: Start date: 16/12/2011 Description: A Proven global CRO leader with more than 11,000 professionals are now open and seeking more ClinicalResearch Associates at various levels to join their Award winning company. Owing to a number of new business wins the UK subsidiary is now going through a period of unprecedented growth and this is your chance to be part of it. You will perform and coordinate all aspects of the clinical monitoring process from start up to close out, including determining protocol and regulatorycompliance of the sites. You will evaluate the quality of study site practices and ensure protocol adherence escalating any quality issues to your PM. The addition to this is that Senior CRA's will have the opportunity to be home based. The candidatessuitable for such role must demonstrate previous Clinical Monitoring experience within Phase II-III studies. You must also havea Nursing equivalent or suitable Degree in life sciences and be in possession of a full Driving licence and speak fluent English. This is an excellent chance to become part of a recognised global CRO (Clinical Research Organisation) and to reward you for your hard work; the company will be offering an excellent salary along with fantastic benefits! For immediate considerationand a full job description please forward your CV to Bradley.doyle@secpharma.com or call + 44 (0) 207 255 6665 Keywords: CRA, Clinical Research Associate, Senior Clinical Research Associate, Lead CRA, Lead Clinical Research Associate, Team Leader, Manager, Diabetes, Obesity, Pain, CNS, HIV, Oncology, Cardiovascular, Respiratory, Therapeutic, Development, Career, Progression, job, role, Study Management, Site Management, CRO, Pharmaceutical, Clinical Operations Industry: Science and Research Salary currency: gbp Salary Benefits: car+pension+health care+Bonus Salary: £26000 - £36000 per annum + car+pension+health care+Bonus Job type: Permanent Job skills: Job Reference: 020391 http://www.hallolondon.co.uk/index.html?op=3&id=774573 Job duration: Start date: 16/12/2011 Description: This leading Contract Research organisation are seeking Clinical Research Associates to join there award winning Clinical Operations department owing to huge growth in the UK with a number of their clients potential blockbuster medicines waiting to be delivered to market. These positions can be based in my client's office or for more experience CRA's there is the option of working field-based. You will perform and coordinate all aspects of the clinical monitoring process fromstart up to close out, including determining protocol and regulatory compliance of the sites. You will evaluate the quality of study site practices and ensure protocol adherence escalating any quality issues to your PM. The addition to this is that SeniorCRA's will help with professional development for those who are less experienced and all activities will be ensured to follow ICH-GCP guidelines. The candidates suitable for such role must demonstrate previous Clinical Monitoring experience within PhaseII-III studies. You must also have a Nursing equivalent or suitable Degree in life sciences and be in possession of a full Driving licence and speak fluent English. In return my client can offer you a competitive salary and remuneration package the opportunity for fast-track career progression and potentially the opportunity to work in a regional monitoring capacity creating agreater work:life balance. For immediate consideration and a full job description please forward your CV to Bradley.doyle@secpharma.com or call + 44 (0) 207 255 6665 Keywords: CRA, Clinical Research Associate, Senior Clinical Research Associate, Lead CRA, Lead Clinical Research Associate, Team Leader, Manager, Diabetes, Obesity, Pain, CNS, HIV, Oncology, Cardiovascular, Respiratory, Therapeutic, Development, Career, Progression, job, role, Study Management, Site Management, CRO, Pharmaceutical, Clinical Operations Industry: Science and Research Salary currency: gbp Salary Benefits: car+bonus+pension+health care Salary: £25000 - £40000 per annum + car+bonus+pension+health care Job type: Permanent Job skills: Job Reference: 010391 http://www.hallolondon.co.uk/index.html?op=3&id=774564 Job duration: Start date: ASAP Description: SEC/Ref: 110620G1 Senior Statistical Programmer| Perm | UK SE England and Scotland - Competitive Salary + Benefits For immediate consideration please forward your CV to:clive.magill@secpharma.com or call +44 (0) 207 255 6665. Are you a programmer looking to take the next step in you career with an international company who will develop your career? Then look no furthur my client who are seeking programmers to work onglobal clinical trials covering a range of phases and theraputic areas. The role would include being lead programmer on select projects with responsibility to plan and coordinate activities for team members. Summary of job description - Program and QC analysis datasets, pooled datasets, summaries and TFLs for phase I-IV clinical trials - Ensure adherence appropriate standards - Produce good quality SAS programs - Document all work in clear and logical fashion ensuring that program and project documentation are maintained. - Provide programming input into CRFs and data management plans as well as programming aspects of SAPs - Input into estimation of task durations for programming deliverables. - Liaise with internal and external parties on programming aspects of projects. - Perform role of Lead Programmer on selected studies acting as consultant where necessary. - Supervise and train junior team members. Experience Required - Minimum of BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or similar. - Excellent and proven SAS programming skills (BASE, MACRO, GRAPH). - Knowledge andexperience in database structures. - At least 4 years experience in programming in a clinical trials environment or in a related field. - Good knowledge of statistical principals underlying clinical trials. - Working with ICH/GCP and knowledge of regulatory requiremetns is essential. If you would to discuss this role in greater detail or your application / suitability to this or further roles, please contact me. Contact: Clive Magill Consultant - Pharmaceutical, Healthcare & CRO DivisionStatistics, Biostatistics & Programming Tel: +44 (0) 207 255 6665 Email: clive.magill@secpharma.com Website: www.secrecruitment.com http://uk.linkedin.com/pub/clive-magill/30/63a/878 Industry: Science and Research Salary currency: gbp Salary Benefits: Negotiable Salary: £40000 - £50000 per annum + Negotiable Job type: Permanent Job skills: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician, lead, SAS, project Job Reference: SEC/Ref: 110620G1 http://www.hallolondon.co.uk/index.html?op=3&id=766518 Job duration: perm Start date: negotiable Description: Junior Clinical Project Manager-Warsaw-Poland-international CRO-immediate start-15 000 PLN per month+ company car and benefits! A new position of a Clinical Project Manager has just become available in an international Clinical Research Organisation in their Warsaw-based office.For my client I am now looking a professional on a permanent position of a Clinical Project Manager who would be responsible forthe management of international phase II-IV trials in varied therapeutic areas as well as line management of a small team of Clinical Research Associates. This position will suit an experienced Lead Clinical Research Associate who is looking to take another step in their professional career. An ideal candidate will have at least five years experience in clinical research, will bean experienced CRA and will have proven leadership and management skills. Ideally they will have previous mentoring experience.Fluent knowledge of both Polish and English languages is a must. A successful candidate will be rewarded with a permanent position, secure employment and an opportunity to grow within the organisation. They will get a chance to develop their career on management level role, they will work on interesting international trials working alongside enthusiastic international teams. Theywill receive a salary of around 15 000 PLN per a month (negotiable), a company car and a benefits package. At SEC Pharmaceutical Recruitment we are committed to helping Clinical Research Professionals find a role which would meet their expectations. Having extensive industry knowledge and excellent links with hiring managers in CROs, Pharmaceutical Companies and Biotechs throughout Europe we are happy to advise you on the ways to develop your clinical research career. If you are interested in discussing this specific opening, please contact me on (0) 2072556665 for a confidential discussion or for an immediate consideration, forward your CV to agata.lugowska@secpharma.com Key words: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager,Lead CRA, Poland, Polska, Warsaw, Warszawa Industry: Science and Research Salary currency: gbp Salary Benefits: negotiable+benefits Salary: €35000 - €40000 per annum + negotiable+benefits Job type: Permanent Job skills: clinical, project management, CPM Job Reference: 1200012 http://www.hallolondon.co.uk/index.html?op=3&id=763892 Job duration: Start date: 01.01.2012 Description: The primary purpose of this role is to lead and manage domestic or international projects and mayoversee a series of small programs on a particular compound.(will also be part of a global project management team).You will bementoring Associate Project Leaders and Functional Leads for specific projects. You will participate in proposal development teams, giving input to particular indication and operational structure for the proposal alongside of being responsible to represent Project Management at marketing/new business meetings. Part of this role is also support Leadership by developing ways to align people's contribution to business goals and strategic thinking and developing a mentoring and learning behavior for other members involved in the projects. General areas of responsibility include: Sponsor liaison, project assessment and initiation, resource procurement and planning, project implementation, leading and motivating a cross-functional team, milestone planning andtracking, ensuring that projects are progressing according to contract and quality standards, SOPs, ICH-GCP and/or other guidelines to fulfill local regulations, production of key project progress reports, management of communication between company project team, Sponsor, contract and financial management. You as a right candidate, you will have proven substantial relevant experience in healthcare, clinical research, project management or contract research organization. Peri-approval study phase experience necessary with large scale post-marketing, EAP and/or remote monitoring trials. Experience working with research-naive sitesand in providing creative solutions to Sponsor organizations in the post-marketing area. Fluency in local language and Englishis essential. In return you can look for highly competitive salary remuneration, great career potential plus generous bonusesand social benefits. Also please use our referral scheme and get reward up to 200 euros in case that you will recommend candidates with successful placement. For immediate consideration and a full job description please send through your full CV to margareta.hudcovicova@secpharma.com or call + 44 (0) 207 255 6600 Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: €75000 - €80000 per annum Job type: Permanent Job skills: Job Reference: 555555 http://www.hallolondon.co.uk/index.html?op=3&id=762896 Job duration: 6 month Start date: ASAP Description: 201011a FREELANCE: Statistical Programmer - PK/PD Support 3-6 month rolling contract Accountabilities: *Support clinical PK/PD group. *Meet project team timelines *Interact with project team members to understand reporting requirements *Provide programming support for PK/PD modelling and simulation in compliance with relevant SOPs. *Provide programming perspective and input to project team activities which may include: Essential Skills: 5-10 Years SAS programming experience Good CDISC skills (SDTM, ADaM) Excellent communication skills - verbal and written Excellent analytical skills Ability to work independently, as part of a group and ask questions For furtherdetails or a confidential conversation please contact me directly: James Carrera Pharmaceutical Division Statistics, Biostatistics & Programming Tel: +44 (0) 207 255 6665 james.carrera@secpharma.com http://uk.linkedin.com/in/jamescarreraPharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician,biostatistics, biostatistician Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: €65 - €75 per hour Job type: Contract Job skills: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician Job Reference: 20111a http://www.hallolondon.co.uk/index.html?op=3&id=760051 Job duration: 6-12 month Start date: asap Description: Lead Statistician - Phase II - III Based in South East, UK £ Excellent Rate / hour - Dependant on Experience Accountabilities/Responsibilities: *Planning and decision making about state-of-the-art study designs, evaluation methods and sample size calculations; developing study protocols in collaboration with study physicians; participating in the monitoring of study conduct to oversee data quality and potential implications for the planned analysis. *Planning and controlling the entire study evaluation and reporting process through a statistical analysis plan; performing the inferential statistical evaluations *Writing integrated reports and scientific publications, in collaboration with the study physician and medical writer *Planning statistical aspects of clinical development plans, in close collaboration with the medical project leader and other members of theglobal project team. Providing answers to project related statistical or methodological questions from decision-makers inside and outside the company *Writing detailed statistical project plans and stipulating requirements and standards for study teams;providing guidance to study statisticians on protocol development, analysis plans, study report, and publications. *Planning and compiling clinical registration dossiers; preparing regulatory documentation for the EU and the USA, in collaboration with project physicians and data managers; discussing statistical issues with drug regulators. Essential Skills & Capabilities:5-8 years solid experience as a statistician / biostatistician in the Pharmaceutical, Biotech or CRO industry You will be expected to have an MSc or PhD degree in statistics or mathematics as well as a comprehensive knowledge of biostatistics. You should also be familiar with the application of new statistical methods and theories in software solutions involving SAS or S-Plus.Although this is a multiphase role, Oncology experience is highly desirable For further details or a confidential conversation please contact me directly: James Carrera Manager - Pharmaceutical, Healthcare & CRO Division Statistics, Biostatistics & Programming Tel: +44 (0) 207 255 6665 james.carrera@secpharma.com http://uk.linkedin.com/in/jamescarreraPharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £70 - £85 per hour Job type: Contract Job skills: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, progra Job Reference: 201011b http://www.hallolondon.co.uk/index.html?op=3&id=760048 Job duration: 6 months Start date: ASAP Description: For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@secpharma.com IMMEDIATE BUSINESS NEED Excellent Rate - £50-55 / hour 6 month+, Immediate Start Available & preferred, but they will wait for notice Based in SouthEast, UK This position is 100% office-based due to the nature of the work Accountabilities/Responsibilities: - Lead thestatistical programming activities on a project. Provide direction and focus on programming activities related to analysis and reporting of results on the assigned drug development project. - Provide expert knowledge on statistical programming strategies.Assess and clarify requirements, provide statistical programming solutions and ensure their effective implementation. - Guidestatistical programming team members on trial protocol review, CRF development and data structure specifications for clinical trials. Ensure consistency and adherence to available standards. - Oversee the programming specifications within the project andensures consistency with the statistical requirements for analysis datasets, pooled datasets, listings, tables, and figures. Assist as appropriate. - Lead activities on programming, validation and documentation according to the agreed specification, pooled datasets, listings, tables, and figures. Ensure that high quality standards, consistency within the project and delivery within agreed time lines are being met. Assist as appropriate. - Ensure adherence to statistical programming standards, effective use of available standard programs, availability of appropriate documentation and compliance with Standard Operating Procedures.- Act as PoC, liaising with sponsors, customers and other functional areas as required. Essential Skills & Capabilities:- At least 6 years of pharmaceutical industry drug development experience using SAS. - Expert knowledge of SAS programminglanguage, with SAS/Base, SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS. - Good knowledge of drug development process in particular on collection, storing, processing and analysis of clinical trial data. - Good knowledge of English, communicating clearly and effectively in written and oral form in a business environment. - Well developed planning , organizational and analytic abilities - Strong customer focus For a confidential consultation call; James Carrera Statistics, Biostatistics & SAS Programming Pharmaceutical Division Tel: +44 (0)20 7255 6600 Fax: +44 (0)20 7255 6656 Email: James.Carrera@secpharma.com Web: www.secrecruitment.com 3rd Floor, Woolverstone House, 61-62 Berners Street London W1T 3NJ United Kingdom SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: £50 - £55 per hour Job type: Contract Job skills: sas statistical programmer base macro clinical pharma pharmaceutical Job Reference: 920/11a http://www.hallolondon.co.uk/index.html?op=3&id=760047 Job duration: perm Start date: negotiable Description: Clinical Research Associate-permanent role-Warsaw office-international Clinical Research Organisation-immediate start! My client, a full service CRO with extensive experience in clinical research and established presence in Europe Asia and America, is providing end-to-end services for Phase II- IV clinical research. My client's service quality, therapeutic expertise and global reach have allowed them to grow rapidly and to build alist of prestigious clients all over the world. They are now giving you an opportunity to join their successful team workingas a Senior Clinical Research Associate with monitoring responsibilities in Poland. Working as a Senior CRA you will be mainly responsible for monitoring on every stage of the trial, investigators recruitment, study budget negotiations, reviewing clinical documents, mentoring and training of more junior CRAs. A full job description will be provided upon application. Candidates will need to be experienced Clinical Research Associates with outstanding leading skills and a strong motivation to developtheir career within clinical research. In return my client offers a very competitive salary combined with numerous benefits, dedicated training scheme and a great working environment. Due to company's continuous expansion ideal candidates will be offereda chance to progress within the organisation. For logistical reasons my client is limited their search to candidates already living within the EMEA region at this time. At SEC Pharmaceutical Recruitment we are committed to helping Clinical Research Professionals find a role which would meet their expectations. Having extensive industry knowledge and excellent links with hiring managers in CROs, Pharmaceutical Companies and Biotechs throughout Europe we are happy to advise you on the ways to develop yourclinical research career. If you are interested in discussing this specific opening, please contact me on (0) 2072556665 for a confidential discussion or for an immediate consideration, forward your CV to agata.lugowska@secpharma.com Key words: Clinical Research Associate, CRA, CRO, Clinical Research Organisation, Warsaw, Warszawa, Mazowieckie. Industry: Science and Research Salary currency: gbp Salary Benefits: negotiable Salary: negotiable Job type: Permanent Job skills: clinical, cra, monitoring Job Reference: 1255512 http://www.hallolondon.co.uk/index.html?op=3&id=754593 Job duration: Start date: 01.01.2012 Description: The primary purpose of this role is to lead and manage domestic or international projects and mayoversee a series of small programs on a particular compound.(will also be part of a global project management team).You will bementoring Associate Project Leaders and Functional Leads for specific projects. You will participate in proposal development teams, giving input to particular indication and operational structure for the proposal alongside of being responsible to represent Project Management at marketing/new business meetings. Part of this role is also support Leadership by developing ways to align people's contribution to business goals and strategic thinking and developing a mentoring and learning behavior for other members involved in the projects. General areas of responsibility include: Sponsor liaison, project assessment and initiation, resource procurement and planning, project implementation, leading and motivating a cross-functional team, milestone planning andtracking, ensuring that projects are progressing according to contract and quality standards, SOPs, ICH-GCP and/or other guidelines to fulfill local regulations, production of key project progress reports, management of communication between company project team, Sponsor, contract and financial management. You as a right candidate, you will have proven substantial relevant experience in healthcare, clinical research, project management or contract research organization. Peri-approval study phase experience necessary with large scale post-marketing, EAP and/or remote monitoring trials. Experience working with research-naive sitesand in providing creative solutions to Sponsor organizations in the post-marketing area. Fluency in local language and Englishis essential. In return you can look for highly competitive salary remuneration, great career potential plus generous bonusesand social benefits. Also please use our referral scheme and get reward up to 200 euros in case that you will recommend candidates with successful placement. For immediate consideration and a full job description please send through your full CV to margareta.hudcovicova@secpharma.com or call + 44 (0) 207 255 6600 Industry: Science and Research Salary currency: gbp Salary Benefits: Salary: €75000 - €80000 per annum Job type: Permanent Job skills: Job Reference: 555555 http://www.hallolondon.co.uk/index.html?op=3&id=751446 Job duration: Start date: ASAP Description: SEC/Ref: 110620G Senior Statistical Programmer| Perm | UK SE England and Scotland - Competitive Salary + Benefits For immediate consideration please forward your CV to:clive.magill@secpharma.com or call +44 (0) 207 255 6660. My clients are seeking programmers to take responsibility for programming aspects of global clinical trials across all phases and multi-ple theraputic areas. These roles would include being lead programmer on selected projects with responsibility to plan and coordinate activities for assigned team members. Summary of job description - Program and QC analysis datasets, pooled datasets, listings, summaries, figures and tables for phase I-IV clinical trials and for overall summaries of safety and efficacy. - Production and QC of study specifications for analysis datasets and pooled datasets. - Provide input as appropriate into specifications for data listings, data summaries/tables and figuresfor phase I-IV clinical trials, and for overall summaries of safety and efficacy, to ensure adherence appropriate standards - Produce good quality SAS programs - Document all work in clear and logical fashion ensuring that program and project documentation are maintained. - Provide programming input into CRFs and data management plans as well as programming aspects of SAPs - Input into estimation of task durations for programming deliverables. - Liaise with internal and external parties on programmingaspects of projects. - Perform role of Lead Programmer on selected studies acting as consultant where necessary. - Superviseand train junior team members. Experience Required - Minimum of BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or similar. - Excellent and proven SAS programming skills (BASE, MACRO, GRAPH). - Knowledge and experience in database structures. - At least 4 years experience in programming in a clinical trials environment or in a related field. - Good knowledge of statistical principals underlying clinical trials. - Working with ICH/GCP and knowledge of regulatory requiremetns is essential. If you would to discuss this role in greater detail or your application / suitability to this or further roles, please contact me. Contact: Clive Magill Consultant - Pharmaceutical, Healthcare & CRO Division Statistics, Biostatistics & Programming Tel: +44 (0) 207 255 6660 Email: clive.magill@secpharma.com Website: www.secrecruitment.com http://uk.linkedin.com/pub/clive-magill/30/63a/878 Industry: Science and Research Salary currency: gbp Salary Benefits: Negotiable Salary: £40000 - £50000 per annum + Negotiable Job type: Permanent Job skills: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician, lead, SAS, project Job Reference: SEC/Ref: 110620I http://www.hallolondon.co.uk/index.html?op=3&id=749670