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Hiring Clinical Trial Assistant (CTA) | Work From Home
Syneos Health
Remote (India)
0–2 Years
Clinical Research
🏢 About Syneos Health
Syneos Health is a global CRO supporting clinical development and commercialization. The company is involved in a large percentage of global drug approvals and offers strong career growth in clinical research.
📋 Job Overview
- Role: Clinical Trial Assistant (CTA)
- Location: Remote (India)
- Experience: 0–2 Years
- Type: Full-Time (Future Pipeline Role)
- Department: Clinical Operations
📌 Key Responsibilities
- Assist clinical monitoring teams
- Maintain Trial Master File (TMF)
- Track regulatory & clinical documents
- Support site communication
- Manage CRF tracking & queries
- Handle trial databases & systems
- Coordinate logistics & documentation
- Attend meetings & prepare minutes
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / Pharm.D / BSc / MSc
- Life Sciences / Biotechnology background
- Basic clinical research knowledge
- Good communication skills
💰 Salary (Estimated)
- ₹3 LPA – ₹5.5 LPA
- (Based on entry-level CRO roles in India)
🎯 Why This Role is Important
- Entry into global CRO industry
- Work from home opportunity
- Career path → CRA / CDM / Regulatory
📚 Internal Resources (Must Read)
🎯 Interview Tips
- Revise ICH-GCP basics
- Understand clinical trial phases
- Focus on documentation questions
- Improve communication skills
📚 Practice:
📌 Note Before You Apply:
This is a future pipeline role. Apply early to increase your chances of selection.
This is a future pipeline role. Apply early to increase your chances of selection.
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Since this is for pipeline/future clinical operations roles, ensure your profile and qualifications align with clinical trial assistant workflows, study tracking coordination, Trial Master File (TMF/eTMF) documentation support, site management assistance, and ICH-GCP regulatory guidelines compliance standards before proceeding with your application on the Syneos Health portal.
Kindly read the full job description carefully before applying. Since this is for pipeline/future clinical operations roles, ensure your profile and qualifications align with clinical trial assistant workflows, study tracking coordination, Trial Master File (TMF/eTMF) documentation support, site management assistance, and ICH-GCP regulatory guidelines compliance standards before proceeding with your application on the Syneos Health portal.
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