Syneos Health has announced an excellent opportunity for experienced clinical research professionals to join as a Project Associate (Clinical) in Hyderabad, India. This hybrid opportunity is ideal for candidates with 1โ2 years of clinical research experience who want to build a career in Clinical Trial Management, Clinical Operations, and Project Management within a leading global CRO.
The Project Associate will work closely with Clinical Project Leads to support the planning, execution, documentation, financial tracking, timelines, and quality management of global clinical trials. Candidates with experience in CTMS, Trial Master File (TMF), ICH-GCP guidelines, and clinical project coordination are encouraged to apply.
If you’re looking for Syneos Health Project Associate Clinical Jobs 2026, this opportunity offers excellent career growth, exposure to international clinical trials, and the chance to work with one of the world’s leading biopharmaceutical solutions organizations.
Job Overview
| Particular | Details |
|---|---|
| Company | Syneos Health |
| Position | Project Associate (Clinical) |
| Job Type | Full-Time |
| Work Mode | Hybrid |
| Location | Hyderabad, India |
| Shift | 8:00 PM โ 5:00 AM IST (3rd Shift) |
| Experience | 1โ2 Years |
| Qualification | Bachelor’s Degree |
| Industry | Clinical Research / CRO |
Key Responsibilities
As a Project Associate (Clinical), you will:
- Support planning and execution of clinical trials alongside Project Leads.
- Coordinate clinical study activities across multiple teams.
- Track project timelines and ensure milestones are achieved.
- Maintain project documentation and clinical trial records.
- Prepare and distribute study-related financial reports.
- Monitor project budgets and financial health.
- Coordinate with vendors and internal stakeholders.
- Document project scope, risks, and mitigation plans.
- Escalate project issues and ensure timely resolution.
- Maintain CTMS, TMF, PDC, SOPNet and other project systems.
- Support audit readiness and quality assurance activities.
- Ensure compliance with ICH-GCP guidelines and SOPs.
- Assist in project communications across global teams.
Eligibility Criteria
Candidates should possess:
- Bachelor’s degree in:
- B.Pharm
- M.Pharm
- Life Sciences
- Nursing
- Medicine
- Clinical Research
- Project Management
- Related Healthcare Discipline
Experience Required
- 1โ2 years of experience in Clinical Research or Clinical Operations.
- Experience supporting clinical trials is mandatory.
Required Skills
Applicants should have knowledge of:
- Clinical Trial Management System (CTMS)
- Trial Master File (TMF)
- Project Delivery Center (PDC)
- SOPNet
- Clinical Trial Documentation
- ICH-GCP Guidelines
- Clinical Project Coordination
- Microsoft Office Suite
- Project Management Tools
- Stakeholder Communication
- Budget Tracking
- Risk Management
- Audit Preparation
- Documentation Management
- Excellent Written & Spoken English
Why Join Syneos Health?
Working at Syneos Health offers:
- Hybrid work model
- Global clinical trial exposure
- Career progression opportunities
- International project experience
- Learning & development programs
- Competitive compensation
- Inclusive work culture
- Global collaboration across 110+ countries
- Exposure to innovative clinical research projects
Work Schedule
- Third Shift
- 8:00 PM โ 5:00 AM (Indian Standard Time)
Who Should Apply?
This opportunity is suitable for professionals working as:
- Clinical Trial Coordinator
- Clinical Project Coordinator
- Clinical Operations Associate
- Project Associate
- Clinical Research Associate (CRA)
- Clinical Trial Assistant (CTA)
- Clinical Project Executive
- Clinical Documentation Specialist
Important Note
This posting is for Syneos Health’s talent pipeline and may not represent an immediately available opening. Candidates expressing interest will be considered for future Project Associate (Clinical) opportunities.
How to Apply
