One of the biggest Pharmaceutical firm is aiming to bring on an Associate Director, Statistical Programmer in the New Jersey area to assist in helping make a difference in the pharmaceutical industry. They will spearhead the statistical programming activities for multiple studies and will lead the programming submission related activities. Additionally, this position will work with the Head of programming to establish standards for programming and establish efficiency within the group.
The Associate Director will be responsible for:
* Collaborating with the Head of programming to establish standards for programming and establish efficiency within the group.
* Overseeing SAS programming activities in support of Multiple Studies
* Serve as the key "go to" Subject Matter Expert for all Statistical Programming issues in a highly specialized yet collegiate corporate environment
* Supporting multiple studies such as Phase II -IIIB for a single or multiple compound within related therapeutic areas spanning inception through to submission
The Associate Director should have the following qualifications:
* BS or MS in relevant field; MS degree preferred
* 8+ years of statistical programming experience or equivalent.
* Advance knowledge of Regulatory & Compliance Requirements for Biostatistics processes
* Solid leadership skills, including management of people resources, FTEs, Contractors, and/or CRO vendors within a matrixed environment
* Possess TA experience in epilepsy, Neurodegenerative disease, sleep disorders, cardiovascular or inflammatory disease.
Benefits:
* Excellent Benefits Package (Health, Dental, 401k, Stock Option etc.)
* Health and Wellness programs
* Generous PTO plan
If you are interested in the Senior Principal Statistician role, then please don't wait to apply.
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Associate Director, Statistical Programming
- Location New Jersey
- Job type Permanent
- Salary US$140000 - US$160000 per year
- Discipline Biometrics
- Reference PR/272841_1597872086