Clinical Trial Associate at Takeda
Location: Gurgaon, Haryana
Organization: Takeda Global
Position: Clinical Trial Associate
Experience: 3 Years
Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, BSc in Life Sciences
Salary: Not disclosed
About Takeda
Takeda is a global biopharmaceutical company focused on improving global health through innovation. Join us to impact lives and contribute to sustainable healthcare.
Responsibilities
- eTMF Management: Oversee eTMF creation and quality.
- Documentation Compliance: Ensure adherence to regulatory guidelines and specifications.
- System Oversight: Track eTMF patterns and respond to system inquiries.
- Audit Assistance: Support audits and inspections.
- CRO Oversight: Assist in managing CRO relationships.
- CTMS Setup: Collaborate on program and venue setups.
- Meeting Coordination: Organize meetings to ensure CTMS functionality.
Qualifications
- Bachelor’s degree in a relevant science or healthcare field.
- 3+ years in clinical research and TMF, ideally in pharmaceutical, biotech, or CRO settings.
- Experience with Veeva Vault CTMS & eTMF or similar software is a plus.
- Knowledge of local clinical trial laws and GCP.
- Strong problem-solving, communication, and organizational skills.
- Proven track record of success.
How to Apply
- Visit the Takeda Careers Portal.
- Search for Job ID R0120735 in the Research & Development section.
- Click “Apply” and ensure your information is accurate and up-to-date.
Join Takeda to be part of a team driving innovative research and improving patient outcomes!