Perform biometrics and SAS programming activities for all clinical trials involving drugs, biologics and devices, and oversees the activities of programming and biostatistician consultants....
* Responsible for the development of clinical trial data management plan, assist in developing research programs and CRF table design
In charge of organization and management of clinical trials...
Ph.D. in Statistics/Biostatistics with at least 5 years of experience in the pharmaceutical industry, or an M.S. degree with at least 8 years of experience in the pharmaceutical industry...
Roles and Responsibilities
Lead a team of SAS programmers & OC programmers and set priorities and timelines for programming deliverables based on project requirements
As a team leader,...
Your profile:
- You have several years of experience in planning, evaluation and reporting of clinical trials phase I to IV
- They are flexible and can work temporarily in other places (Germany,...
Responsibilities:
• Development and application of new biometric and bioinformatic methods
• Statistical planning and evaluation of medical research / experimental and clinical studies...
Scientist / researcher
Application Deadline: 28 June 2010
Responsibilities:
Biometric expert evaluation of documents submitted in support of requests by pharmaceutical companies in the...