Thermo Fisher Scientific Inc. is a global leader in scientific research, healthcare, and pharmaceuticals, committed to making the world healthier, cleaner, and safer. With a strong presence in over 50 countries, Thermo Fisher provides cutting-edge solutions in clinical trials, diagnostics, and biotechnology. The company fosters innovation, diversity, and professional growth, making it a top employer in the life sciences sector.

Job Openings

1. Country Approval Specialist (Fully Remote, India)

Job ID: R-01321978 | Work Schedule: Mon-Fri | Location: Remote, India

Key Responsibilities:

• Manage regulatory & ethics committee submissions for clinical trials in India.
• Ensure compliance with ICH-GCP, Indian regulations, and study startup timelines.
• Collaborate with CRAs, Clinical Trial Managers, and regulatory teams.
• Prepare and review site contracts, budgets, and essential documents.
• Maintain accurate records of approvals and documentation.

Eligibility:

• Experience in study startup, regulatory affairs, or clinical operations.
• Strong knowledge of Indian clinical trial regulations & GCP guidelines.
• Excellent organizational, communication, and negotiation skills.
• Ability to work in a fast-paced, cross-functional team.

Educational Qualification (Degree):

• Bachelor’s or Master’s degree in one of the following fields:
  • Pharmacy (B.Pharm / M.Pharm)
  • Life Sciences (B.Sc / M.Sc in Biotechnology, Microbiology, Biochemistry, etc.)
  • Medicine (MBBS, BDS, BAMS, BHMS)
  • Nursing (B.Sc Nursing)
  • Other health/science-related fields

Experience Required:

• 2 to 5+ years of relevant work experience in study startup, clinical operations, or regulatory affairs in the pharmaceutical, CRO (Contract Research Organization), or biotech industry.

2. CRA Level II (Mumbai/Remote, India)

Job ID: R-01321868 | Work Schedule: Mon-Fri | Location: Mumbai/Remote

Key Responsibilities:

• Conduct on-site & remote monitoring for clinical trials.
• Ensure protocol compliance, ICH-GCP adherence, and data accuracy.
• Perform SDV, SDR, and investigational product reviews.
• Manage site relationships, regulatory documents, and audit readiness.
• Support trial close-out activities and risk-based monitoring.

Eligibility:

• Bachelor’s degree in Life Sciences / Nursing or related field.
• 3-5 years of onsite monitoring experience as a CRA.
• Strong knowledge of ICH-GCP, regulatory guidelines, and clinical processes.
• Excellent analytical, communication, and problem-solving skills.

Why Join Thermo Fisher Scientific?

✅ Global Impact: Contribute to groundbreaking healthcare & research projects.
✅ Career Growth: Opportunities for professional development & leadership.
✅ Work Flexibility: Fully remote & hybrid work options available.
✅ Inclusive Culture: Diverse, collaborative, and innovation-driven environment.
✅ Competitive Benefits: Health insurance, performance bonuses, and more.

How to Apply

Application Link For Country Approval Specialist (Fully Remote, India)

Application Link For CRA Level II