Dear Allstat,
CK Clinical are currently handling both permanent and contractual vacancies with a number of pharmaceuticals/CRO's in the UK and EU. Below are a selection of roles on offer, please note salary/rates for the advertised positions are competitive but negotiable and will be discussed upon application.
Statistical Programmer (Pharmaceutical)
Contract - 6 months +
UK
The purpose of the role is to provide a comprehensive statistical service for the Company and be responsible for all statistical aspects of the 5-6 clinical trials to which you will be independently managing.
* Designing statistical studies for the analysis of clinical trials; formulating the hypotheses and objectives.
* Providing a statistical quality control service while studies are in progress.
* Assessing the impact on the statistical analysis of changes made during the study.
* Performing the statistical analyses of clinical trials and answer statistical queries on the analysis or results.
Interested applicants will hold a minimum of an MSc in Medical Statistics (Or equivalent) with proven experience of working within the Pharmaceutical industry. You will hold excellent SAS Programming skills with a good understanding of CDISC.
Project Statistician (Pharmaceutical)
Contract - 12 months
UK/EU
The purpose of the role is be involved in the development of protocol designs, clinical plans, and data analysis plans.
* Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.
* Collaborate with team members to write reports and communicate results.
* Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.
* Respond to regulatory queries and to interact with regulators.
You will hold either an MSc or PhD in Statistics, Biostatistics OR Equivalent and will have proven industrial experience of working for either a Pharmaceutical/Biotechnology/CRO organisation. You will also be proficient in the SAS programming language.
Senior SAS Programmer (Bio-Pharmaceutical)
Permanent
UK
The purpose of this role is to provide statistical programming expertise in the production of derived analysis-ready data, and to support documentation from assigned clinical trial data following industry standards.
* Lead responsibility for the statistical programming of analysis ready datasets, tabulations, graphics and listings of clinical trial data according to company standards.
* Development of programming specifications for analysis datasets and deliverables in consultation with the Trial Statistician.
* Provide QC of assigned trial data, tabulations, graphs and listings of clinical trial data according to company and regulatory (ICH-GCP) validation standards.
* Develop, validate and maintain company standards and processes in order to ensure efficiency, consistency and traceability between and within studies.
You will be qualified to BSc level (OR Equivalent) in Computing or another related discipline with proven experience of working as a SAS Programmer within the Pharmaceutical/CRO/Biotechnology industry. You will hold excellent knowledge of statistical concepts together with an understanding of industry technical standards, specifically CDISC and other relevant regulatory guidelines.
Senior Statistician (Pharmaceutical)
Contract 6 months +
EU
The purpose of the role is to be responsible for all statistical tasks within studies in the Oncology therapy area.
* Tracking clinical trial / allocated project activities and milestones.
* Be responsible for all statistical tasks of the assigned clinical studies e.g. clinical trial design/planning, analysis plan, reporting activities, support to publications, and any statistical consultation during the running phase
* Ensuring timelines and adequate quality of all Biostatistics and Statistical Reporting deliverables for the assigned trials and project task.
* Following processes and adhering to project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, full development project specifications, and regulatory guidelines)
You will hold at least an MSc in Statistics (OR Equivalent) and proven industrial experience within the Pharmaceutical field. You will also have excellent knowledge of Statistical software packages including SAS and good knowledge of the drug development process; and knowledge of S+
Senior SAS Programmer (Pharmaceutical)
Contract 6 months +
EU
The purpose of the role is to provide programming expertise to assigned projects.
* Program according to specifications, analysis datasets, pooled datasets, listings, and figures for phase I-IV clinical trials and submission activities.
* Support quality control and quality audit of deliverables.
* Develop and comply with project/study programming standards and specifications following internal guidelines.
* Provide input into study protocol, CFR and data structure.
You will be experienced in using SAS in the analysis and the reporting of pharmaceutical data, you will have proven experience in SAS programming with a working knowledge of database design/structures.
Senior SAS Programmer (CRO)
Permanent
UK or EU
The purpose of the role is to plan, develop and validate study level programs. You will also design and develop standard project/department macro programs and data structures whilst providing technical support to SAS users.
* To be responsible for the planning, development and execution of project level programs.
* Maintenance of documentation and files according to departmental policy.
* Develop, maintain and validate standard data structure and software.
* Design and write standard departmental macros/programs that are maintainable, supportable, user friendly and well-documented.
* Monitor procedures for program development and validation.
* Provide Technical Support.
You will hold a BSc in in Scientific discipline with proven experience as a SAS Programmer, having familiarity with multiple software products and platforms.
For a confidential discussion on any of the above roles, please contact Priya Mukherjee on 01438 870028 or email an updated CV to [log in to unmask]
Alternatively, if you would like to discuss any other Statistics or Statistical Programming opportunities, please feel free to contact me.
About us:
CK Clinical is a leading clinical recruitment company handling jobs in clinical research and drug development. Our clients include some of the top Pharmaceutical and Biotechnology companies from around the world and our reputation for honesty and integrity is well known. We offer contract and permanent job opportunities within Clinical Data Management, Clinical SAS Programming, Clinical Statistics, Clinical Coding, CRF Design, Database Build, and EDC Technology.
Best wishes,
Priya
Priya Mukherjee BSc (Hons) MRec CertRP
Senior Consultant
CK Clinical Limited
9 High Street
Stevenage Old Town
Hertfordshire
SG1 3BG
DD: +44 (0)1438 870028
Tel: +44 (0)1438 743047
Fax:+44 (0)1438 723800
www.pharmatimes.com/recruiter-enter <http://www.pharmatimes.com/recruiter-enter>.
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