Ockham is a global provider of resources to the Biotechnology and Pharmaceutical Industry. We work with companies involved with clinical trials and other market approval processes to help them deliver their products on time and on budget. One of our clients in Lawrenceville, NJ is looking for a Statistical Clinical Programmer . This is a contract position.
Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions.
Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead.
Able to support multiple protocols independently and to contribute to integrated summaries of efficacy and safety.
Demonstrates strong SAS programming skills; participates in protocol team and some project team interactions.
Builds successful relationships and seamless interfaces at the protocol/project team level.
Provides timely and effective communication to the programming and statistics leads.
Requirements
5 - 7 years of experience.
Candidates must have strong CDISC: SDTM experience as well as Phase I PK/PD experience.
Master Degree.
Phase I-IV clinical development w/strong working knowledge of pharmacokinetics & pharmacodynamics.
Demonstrated experience required processing data from multiple studies.
Experience in SDTM/CDISC .
Keywords: SAS, SAS Programmer, Statistics, Statistical Programmer, Statistical Analysis, ISS/ISE, Biostatistician, Biostatistical Programmer, Clinical Trials, Clinical Research, Clinical Studies, Pharmaceuticals, Drug Development, IND, NDA, Data Management, Data Manager, Clinical Data Manager, Clinical Data Coordinator, Drug Safety, Drug Safety Specialist, Drug Safety Associate, Pharmacovigilence, Drug Safety Nurse, Drug Safety Physician, Medical Writer, Medical Writing, Regulatory Affairs, Regulatory Submissions, Clinical Project Manager, Clinical Trials Specialist, Medical Services Specialist, BSN, RN, Clinical Research Associate, CRA, Clinical Study Manager, Clinical Study Monitor, Clinical Trials Monitoring, Regional CRA, Regional Clinical Research Associate, In-house CRA, In-house Clinical Research Associate, CDISC, SDTM, ADaM, Rave, Medidata, InForm, Home based, telecommuting, ASG, Ockham
Ockham Development Group Inc - 11 months ago
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