Description
New Contract Opportunities!Global Pharmaceutical
Central New Jersey
12 month contract
Rate is open (please include your rate)
Main purpose of the job:
To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.
Main duties/responsibilities:
1. Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress
2. Developing and maintaining SOPs, SWPs and other related technical documents, providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management. Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents. Determining and researching SAS software upgrades and related systems and addressing maintenance issues.
3. Managing and developing team, maintaining standards for programming activities, and guiding/coaching Statistical programmers.
4. Working independently to accomplish tasks and goals defined by supervisor. Attending required training and meetings and bringing in new ideas to improve the programming process.
Qualifications and education required:
Minimum of Bachelor's degree in Statistics, Computer Science, Mathematics, or a related science discipline. Masters preferred.
Experience required:
Minimum 5 years experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. 7+ years experience preferred.Some project experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment.Understanding of FDA guidelines.Strong verbal, written and interpersonal communication skills needed
Please send me an updated resumes ASAP! Referrals for this job is welcome and appreciated.
Thanks
Paul Dai
To find out more about Real please visit www.realstaffing.com