Global CRO leader Parexel is hiring Study Startup Associates in Bengaluru for professionals with experience in clinical research, site activation, regulatory submissions, and study startup operations. Candidates with expertise in IRB/IEC submissions, CTMS, eTMF systems, and ICH-GCP guidelines are encouraged to apply.
This latest Parexel job opening is an excellent opportunity for life sciences and clinical research professionals looking to grow in the pharmaceutical and biotechnology industry.
About Parexel
Parexel Official Website is one of the world’s leading Clinical Research Organizations (CROs), supporting biopharmaceutical companies in drug development, clinical trials, and regulatory consulting services globally. The company is known for its strong presence in clinical operations, study startup, regulatory affairs, and decentralized trial management.
Job Details
| Particulars | Details |
|---|---|
| Job Role | Study Startup Associate |
| Company | Parexel |
| Location | Bengaluru, Karnataka, India |
| Experience Required | 1–6 Years |
| Employment Type | Full Time |
| Industry | Pharmaceutical & Life Sciences |
| Department | Research & Development |
| Role Category | Pharmaceutical & Biotechnology |
| Openings | 10 |
Primary Keywords
- Parexel jobs in Bengaluru
- Study Startup Associate jobs
- Clinical research jobs in India
- Site activation jobs
- Regulatory submission jobs
- CRO jobs in Bengaluru
- Clinical trial startup associate jobs
- Pharma jobs for life sciences professionals
Job Responsibilities
The selected candidates will manage end-to-end study startup activities and support timely site activation for clinical trials.
Key Responsibilities
- Manage feasibility assessments and site identification activities.
- Prepare and submit IRB/IEC/EC dossiers for regulatory approvals.
- Track amendments, renewals, and ethics committee approvals.
- Coordinate site activation milestones before patient enrollment.
- Review and manage Informed Consent Forms (ICFs), translations, and amendments.
- Maintain accurate study documentation in CTMS and eTMF systems.
- Act as the Single Point of Contact (SPOC) for assigned sites and countries.
- Collaborate with legal, contracts, project management, and clinical teams.
- Identify startup risks and support mitigation strategies to maintain timelines.
Eligibility Criteria
Educational Qualification
- Graduation in Life Sciences, Pharmacy, Biotechnology, or related fields preferred.
Experience Required
- 1–6 years of experience in:
- Clinical Research
- Study Start-Up
- Site Activation
- Regulatory Affairs
Required Skills
Candidates should have knowledge of:
- ICH-GCP guidelines
- IRB/IEC submission processes
- Clinical trial regulatory documentation
- CTMS and eTMF systems
- Veeva Vault
- Oracle or Siebel platforms
- Site activation workflows
- Stakeholder communication and coordination
Why Join Parexel?
Working at Parexel offers strong career growth opportunities in global clinical research operations.
Benefits
- Opportunity to work with international clinical trial teams
- Exposure to global regulatory processes
- Career progression in study startup and clinical operations
- Collaborative work culture
- Experience with leading CTMS/eTMF platforms
- Stable long-term pharmaceutical industry career path
How to Apply
