Job Description

Who are we?

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!



To ensure all assigned studies follows SOPs, GCP and applicable regulations

To do all regulatory/ethics submission as per timelines and to ensure regulatory documents are available, complete and current

In coordination with the project manager and/or medical monitor, perform study site selection visits. Participate in/conduct investigator's meeting and site initiation visits

To perform regular monitoring visits to site

To verify the case report forms and source data according to the monitoring plan

To ensure site level metrics (i.e. 100% IP accountability, 100% informed consent documentation etc.) are tracked and communicated as appropriate

Conduct site close out and assure appropriate archival of controlled documents

Resolve issues as they affect clinical plan timelines and quality to ensure achievement of goals and objectives at the site level

Work in liaison with the finance department in the organization and administration of financial payments to the investigators or relevant local institutions

To ensure the compliance to ICH-GCP guidelines, local & international regulations (Ex. DCGI, FDA) and applicable SOP

Qualifications

• M.Pharm pharmacology / B.Pharm+M.Sc. in Clinical Research

• Should have 5-7 Years' experience of monitoring clinical trials.

• Experience in monitoring the clinical trials which includes SIV, SMV, SCV & Site selection visit

• Travelling included (10-15 days in a month) across India to various cities

Function

Research & Development

Sub Function

Clinical Research

Already Working @TEVA?

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Teva's 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.