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Torrent Pharma Hiring Clinical Research Executive

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Looking to build a career in clinical research and biopharmaceutics? Torrent Pharmaceuticals has announced multiple openings for the role of Executive – Clinical Research (BA/BE studies) in Ahmedabad/Gandhinagar. This opportunity is ideal for M.Pharm (Pharmacology) professionals with hands-on experience in bioavailability (BA) and bioequivalence (BE) studies, pharmacokinetics, and regulatory submissions.

With increasing regulatory focus on ANDA filings, BA/BE study design, and PK evaluation, this role offers strong exposure to both scientific and regulatory aspects of drug development.

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📌 Job Overview

  • Role: Executive – Clinical Research (Biopharmaceutics)
  • Company: Torrent Pharmaceuticals
  • Location: Ahmedabad / Gandhinagar, India
  • Experience: 2–7 Years
  • Qualification: M.Pharm (Pharmacology)
  • Openings: 4
  • Employment Type: Full-time

🔬 Key Responsibilities

As a Clinical Research Executive (Biopharmaceutics), you will:

  • Design and conduct bioavailability (BA) and bioequivalence (BE) studies for oral and non-oral products
  • Perform literature search and protocol development aligned with global regulatory guidelines
  • Coordinate with CROs (Contract Research Organizations) in India and internationally
  • Review BA/BE study protocols, ensuring compliance with pharmacokinetic (PK) principles
  • Monitor pilot and pivotal clinical studies
  • Evaluate study results across:
    • Physicochemical parameters
    • Biopharmaceutics
    • Pharmacokinetics
    • Clinical and formulation data
  • Prepare scientific justifications and regulatory responses for agencies like DCGI
  • Support ANDA submissions and dossier preparation
  • Participate in due diligence for in-licensing and partnered products

🎓 Qualifications & Skills

  • M.Pharm in Pharmacology (mandatory)
  • 2–7 years experience in BA/BE studies and clinical research
  • Strong knowledge of:
    • Pharmacokinetics (PK)
    • Regulatory guidelines (DCGI, USFDA, etc.)
    • Clinical trial monitoring
  • Experience in protocol writing, regulatory submissions, and CRO coordination
  • Analytical mindset with attention to detail

💼 Why Join Torrent Pharmaceuticals?

  • Work with a leading Indian pharma company known for innovation
  • Exposure to global regulatory submissions (ANDA, dossiers)
  • Hands-on experience in clinical research & biopharmaceutics
  • Opportunity to collaborate with international CROs
  • Strong career growth in drug development and regulatory science

📩 How to Apply

Interested candidates can apply by sharing their updated CV at:

📧 vilshashah@torrentpharma.com

Tip: Mention “Executive – Clinical Research (Biopharmaceutics)” in the subject line for better visibility.

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