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[Freshers] Teva Hiring Clinical Research Scientist

Location: Navi Mumbai, India, 400706

Who We Are:
At Teva Pharmaceuticals, we are united by a common mission: to make good health more affordable and accessible, enriching the lives of millions worldwide. With a presence in nearly 60 countries and a diverse workforce representing various nationalities and backgrounds, we are proud to be the leading manufacturer of generic medicines. Our products, many of which are listed on the World Health Organization’s Essential Medicines List, are taken by at least 200 million people every day. But our quest for innovation and impact continues, and we are always seeking new ways to make a difference with the help of passionate individuals like you.

Job Description:
As a Clinical Research Scientist I at Teva Pharmaceuticals, you will play a crucial role in ensuring the proper conduct of clinical studies, contributing to our mission of advancing global healthcare. From ensuring compliance with regulations to overseeing study protocols and documentation, you will be instrumental in driving forward our commitment to excellence in clinical research.

Responsibilities:

  • Ensure compliance with all applicable regulations and complete required forms before study initiation.
  • Familiarize yourself with the GCP, EC/Sponsor agreed protocol, and Lotus SOPs, adhering to ethical principles outlined in the declaration Of Helsinki.
  • Review and provide timely input on study protocols, CRFs, ICDs, and other relevant documents.
  • Obtain ethics committee approval and address any inquiries or concerns raised by the EC.
  • Conduct or supervise all clinical or medical aspects of the study personally.
  • Train study personnel on protocol, study plan, and trial-related duties.
  • Generate necessary trial-related documents in compliance with the protocol.

Requirements:

  • 0-2 years of experience in Clinical Investigator BABE Studies.
  • Female candidates preferred.
  • MBBS degree.

How You’ll Spend Your Day:
Your day will be filled with meaningful tasks that contribute directly to the success of our clinical research endeavors. From ensuring protocol compliance to conducting or supervising study procedures, you will be at the forefront of advancing healthcare solutions that positively impact lives around the world.

Application Link

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