Are you looking for Clinical Support Specialist jobs in Hyderabad or planning to build your career in clinical operations, clinical trials, and site activation? Syneos Health is hiring Clinical Support Specialist II professionals for its Hybrid office in Hyderabad, India. This full-time opportunity is ideal for candidates with 1โ2 years of clinical operations experience who want to work with one of the world’s leading contract research organizations (CROs).
This role offers hands-on exposure to clinical trial documentation, Trial Master File (TMF), regulatory support, project coordination, clinical systems, AI-enabled tools, and cross-functional collaboration, making it an excellent opportunity for professionals seeking long-term growth in clinical research.
Job Overview
| Details | Information |
|---|---|
| Job Title | Clinical Support Specialist II |
| Company | Syneos Health |
| Job Type | Full-Time |
| Work Mode | Hybrid |
| Location | Hyderabad, Telangana, India |
| Experience | 1โ2 Years |
| Education | Bachelor’s Degree |
| Department | Clinical Operations |
| Job ID | 25106656 |
| Posted Date | June 26, 2026 |
About Syneos Health
Syneos Health is a globally recognized clinical research organization (CRO) providing integrated clinical development and commercialization services to pharmaceutical, biotechnology, and medical device companies worldwide.
The organization has contributed to:
- 94% of Novel FDA-approved drugs over the past five years
- 95% of EMA-authorized medicines
- More than 200 clinical studies
- Over 73,000 research sites
- More than 675,000 clinical trial participants
Working at Syneos Health provides professionals exposure to global clinical research projects while supporting innovative therapies that improve patient lives.
Key Responsibilities
The selected Clinical Support Specialist II will provide operational and administrative support across clinical trial activities.
Major responsibilities include:
- Support clinical operations teams with project coordination
- Maintain shared mailboxes and project communications
- Organize clinical documentation and project files
- Track timelines, milestones, and action items
- Enter and reconcile project data in clinical tracking systems
- Perform document creation, formatting, version control, and quality checks
- Support Trial Master File (TMF) management and filing
- Coordinate document translations through approved vendors
- Generate reports using AI-enabled dashboards and reporting tools
- Ensure inspection-ready clinical documentation
- Assist Clinical Research Associates (CRAs) and Country Regulatory Specialists
- Monitor project budgets and workload
- Follow SOPs, Work Instructions, and compliance requirements
- Complete mandatory clinical research training
- Submit accurate timesheets and project updates
Required Qualifications
Candidates should possess:
- Bachelor’s Degree or equivalent qualification
- 1โ2 years of clinical operations experience
- Good understanding of clinical research processes
- Knowledge of clinical trial setup, maintenance, and closeout
- Familiarity with Trial Master File (TMF)
- Strong communication skills
- Excellent documentation abilities
- Good organizational and multitasking skills
- Ability to work independently and within cross-functional teams
- Problem-solving mindset
- Strong attention to detail
- Adaptability to changing project requirements
Preferred Technical Skills
Ideal candidates should have experience with:
- Clinical Operations
- Clinical Trial Documentation
- Trial Master File (TMF)
- Site Activation Support
- Regulatory Documentation
- Clinical Tracking Systems
- Microsoft Outlook
- Microsoft Excel
- Microsoft Word
- Microsoft PowerPoint
- Documentation Quality Control (QC)
- AI-enabled productivity tools
- Timeline Management
- Project Coordination
- Cross-functional Collaboration
Why Join Syneos Health?
Employees at Syneos Health enjoy numerous career advantages, including:
- Hybrid working model
- Global clinical research exposure
- Career development programs
- Technical and therapeutic training
- Competitive compensation
- Inclusive work culture
- International project opportunities
- Continuous learning environment
- Recognition and rewards programs
- Opportunity to work on innovative drug development projects
Who Should Apply?
This Clinical Support Specialist II role is ideal for:
- Clinical Operations Executives
- Clinical Trial Coordinators
- Site Activation Specialists
- TMF Specialists
- Clinical Documentation Professionals
- Clinical Research Associates seeking operational roles
- Healthcare and Life Sciences graduates with clinical operations experience
How to Apply
