1+ months

Senior Manager Clinical SAS Programming

West Chester, PA 19380
Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. Join us on our journey of growth!

Job Description

The Clinical SAS Programming Senior Manager is responsible to manage the timely and accurate execution of programming components of clinical trials.  The Senior Manager leads and manages completed projects, that involved global tasks or cross functional teams or outsourcing resources. The role may require providing inputs to design and analysis, and report the results of clinical trials including programming rules and mocked T/L/G; In addition, providing all safety claims for new drugs and extension of claims/publication support for our marketed drugs. 

 

This role needs to be onsite in West Chester, PA  3-4 days a week, little travel, experience managing projects desired and no visa sponsorship or relocation assistance available.

 

Essential Duties & Responsibilities:

 

1. Supervise or mentor CROs or outsourcing programmers and manage projects.

2. Providing strong SAS programming support to CDISC based e-submission. Develop, review, and/or perform validation of generic macros Develop.

3. Implement programming standards and comply with regulatory requirements among project team members and across all projects; communicate to management on project status and resource issues.

4. Ensuring the accuracy and validity of the study database (SDTM) and/or analysis database (ADaM).

5. Primary responsible for all programming deliverables for NDA/MAA/IND/PSUR.

 

Qualifications

8+ years of of clinical SAS or related programming  professional experience in pharmaceutical or clinical research required.

B.S. degree or relevant experience required.  Coursework in Statistics, Math, Computer Science desired. 

CDISC experience required

 

Function
Research & Development
Sub Function
Clinical Development
Reports To
In process of validation
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Tevas Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Categories

Posted: 2020-01-01 Expires: 2020-03-23

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Senior Manager Clinical SAS Programming

Teva Pharmaceuticals
West Chester, PA 19380

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