Zydus hiring Biopharmaceutics & Clinical Development – Clinical Trial role | Apply Online
Looking for an exciting R&D Pharma Job in the pharmaceutical industry? Zydus is hiring experienced professionals for a Clinical Trial Job in Biopharmaceutics & Clinical Development at its Ahmedabad R&D facility. This opportunity is ideal for candidates with 2–5 years of experience who are passionate about clinical research, global regulatory compliance, and innovative drug development. Explore the complete job details, eligibility criteria, and application information below.
- Position: Biopharmaceutics & Clinical Development – Clinical Trial
- Location: PTC – MORAIYA, R&D – PTC Ahmedabad, Ahmedabad, Gujarat, India
- Job ID: JOB10784
About the Company
Zydus is one of India’s leading global life sciences companies committed to discovering, developing, manufacturing, and marketing innovative healthcare solutions. With a strong focus on research and development, Zydus operates advanced R&D facilities that support global pharmaceutical innovation, clinical research, and regulatory excellence across multiple international markets.
Key Responsibilities
- Provide clinical support for non-oral dosage forms across global markets.
- Prepare biostudy cost proposals and negotiate study budgets with CROs.
- Conduct literature searches and support clinical study design.
- Perform sponsor representative activities during study execution.
- Review and finalize study plans, protocols, and study documents.
- Handle study initiation, monitoring, and study progress tracking.
- Support regulatory query responses and dossier submissions.
- Review clinical reports and clinical data for accuracy.
- Conduct claim-based efficacy and safety studies through CROs.
- Support alternative clinical study approaches.
- Stay updated with global regulatory requirements and clinical trial regulations.
Qualification
- M Pharm in Pharmacology
- Experience: 2–5 Years
- Experience in Clinical Trials, Clinical Development, or Biopharmaceutics.
- Knowledge of global clinical regulations and dossier submissions.
- Experience with CRO coordination and clinical study monitoring.
- Strong understanding of protocol review, clinical documentation, and regulatory compliance.
Why Join this Role?
- Opportunity to work on global clinical trial projects.
- Exposure to international regulatory markets, including the EU, UK, Canada, Brazil, and Mexico.
- Hands-on experience in clinical development and dossier submissions.
- Work with cross-functional R&D and clinical research teams.
- Excellent career growth in pharmaceutical clinical research.
