Parexel is currently hiring Site Start Up Specialists in Hyderabad for professionals with experience in clinical research and regulatory documentation. This role is ideal for candidates looking to grow in clinical trial start-up, TMF management, and global CRO operations.
About Parexel
Parexel is one of the world’s leading Clinical Research Organizations (CROs), supporting pharmaceutical, biotech, and medical device companies across the full clinical development lifecycle. With a global presence, the company focuses on delivering innovative and patient-focused solutions.
Job Overview
- Company: Parexel
- Role: Site Start Up Specialist
- Location: Hyderabad
- Experience: 1–2 Years
- Qualification: Life Sciences / Pharmacy / Biotechnology / Nursing
- Industry: Clinical Research (CRO)
- Job Type: Full-Time
Key Responsibilities
- Support clinical trial site activation activities
- Manage regulatory documentation and submissions
- Coordinate IRB / Ethics Committee documentation
- Maintain and update Trial Master File (TMF / eTMF)
- Ensure documents are inspection-ready
- Track timelines and provide study updates
- Collaborate with internal teams and external stakeholders
- Ensure compliance with ICH-GCP and regulatory guidelines
Required Skills
- Knowledge of clinical research processes
- Understanding of TMF and eTMF systems
- Familiarity with ICH-GCP guidelines
- Strong documentation and organizational skills
- Good communication and coordination abilities
- Basic knowledge of clinical trials and medical terminology
Preferred Skills
- Site Start-Up experience
- Regulatory documentation handling
- Clinical operations exposure
- Investigator site coordination
- CRO experience
Salary Insight
Estimated Salary: ₹7.5 LPA – ₹11.5 LPA
(Salary may vary based on experience and interview performance)
Benefits & Career Growth
- Work on global clinical trials
- Exposure to international projects
- Career growth in clinical operations
- Learning and certification programs
- Inclusive and professional work culture
- Long-term stability in CRO industry
How to Apply
Apply through the official application link or company career portal
Why This Role Matters
Site Start-Up Specialists play a key role in clinical trials by ensuring all documentation, approvals, and site readiness are in place before study initiation. This makes it a high-impact role in drug development.
FAQs
1. Who can apply?
Candidates with a degree in Life Sciences, Pharmacy, Biotechnology, or Nursing with 1–2 years experience.
2. Is TMF knowledge required?
Yes, understanding of TMF/eTMF systems is important.
3. What does this role involve?
Handling regulatory documents, site activation, and clinical trial coordination.
4. Is this a good CRO job?
Yes, Parexel is a globally recognized CRO with strong career growth.
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