1+ months

Clinical Research Associate

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. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!


We offer a competitive benefits package including Medical, Dental, Vision, and Prescription coverage starting on the first day.  We also offer Disability and Life Insurance, Paid Time Off, 6% match on the 401(k), Employee Stock Purchase Plan and Tuition Assistance. For more information on Teva, check us out at www.tevapharm.com or www.tevausa.com


Tevas Global Research & Development (R&D) organization is devoted to the development of new medicines, devices and combination products that provide meaningful therapeutic benefit to patients worldwide. Combining creativity, scientific rigor and our extensive knowledge on a broad range of technologies, our scientists, engineers, medical doctors and project leaders across the globe use their expertise to innovate novel biologics, biosimilars, small molecule specialty medicines, generics and over-the-counter therapies.


Your positon will be reporting into Associate Director, Global Biosimilar Clinical Operations. As a Clinical Research Associate, you will be responsible for assisting the Clinical Study Manager in conducting activities pertaining to biosimilar  studies for the projects assigned to the Clinical Study Manager.  The Clinical Research Associate might be involved in non-study related activities depending of the needs in the department.
Key responsibilities in your new position as our Clinical Research Associate with Teva:

Conducts monitoring visits as part of sponsor oversight responsibilities ( typically less than 5 visits per study).  This oversight visit insures alignment with policies and procedures of Teva and its CRO partners and in accordance with respective country regulations


  • Maintenance and review of Trial Master File (TMF)
  • Documented review of monitoring reports from SIV, IMV COV and informing the CSM of any critical findings
  • Assist with Management of Investigational Products and Ancillary Supplies
  • Review of study specific documents and Case Report Forms.
  • Responsible for operational study oversight activities as delegated by the CSM
  • Participates in cross-functional teams, locally, to assure timely attainment of project milestones
  • Participates in review of pre-qualification / qualification activities 
  • Perform regular reviews of data according to data review/monitoring guidelines.
  • Participate in monthly data review meetings and assist team as needed




Posted: 2020-12-16 Expires: 2021-03-12

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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Clinical Research Associate

Teva Pharmaceuticals
West Chester, PA 19380

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