Perform biometrics and SAS programming activities for all clinical trials involving drugs, biologics and devices, and oversees the activities of programming and biostatistician consultants....
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,...
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...
* 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...
Scientist / researcher
Application Deadline: 28 June 2010
Responsibilities:
Biometric expert evaluation of documents submitted in support of requests by pharmaceutical companies in the...
Responsibilities:
• Development and application of new biometric and bioinformatic methods
• Statistical planning and evaluation of medical research / experimental and clinical studies...
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,...