The role involves working closely with clinical operations teams to ensure timely project execution, maintain inspection-ready documentation, and support clinical trial activities throughout the study lifecycle.
Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Support Specialist – Site Contracts Dedicated |
| Company | Syneos Health |
| Location | Hyderabad |
| Job Type | Hybrid |
| Experience | Fresher |
| Category / Department | CDM |
| Application Mode | Online |
🏢 About Syneos Health
Syneos Health is a leading global, fully integrated biopharmaceutical solutions organization that supports pharmaceutical, biotechnology, and medical device companies throughout the drug development and commercialization process.
The organization partners with innovators worldwide to accelerate clinical development, improve operational efficiency, and bring life-changing therapies to patients faster. With a global workforce of thousands of professionals, Syneos Health has contributed to the development of the majority of recently approved FDA and EMA therapies while supporting hundreds of clinical studies across thousands of research sites worldwide.
💡 Editor's Note / Preparation Tip
Clinical Operations support roles continue to play a crucial part in the successful execution of global clinical trials. This opportunity at Syneos Health provides professionals with exposure to clinical documentation, Trial Master File management, project coordination, quality processes, and international study operations. Candidates looking to build long-term careers in Clinical Operations, Clinical Trial Management, or Project Management within the CRO industry can benefit from the structured learning environment and global exposure offered by this position.
📝 Job Description
🚀 Syneos Health Hiring for Clinical Support Specialist – Site Contracts Dedicated | Hyderabad | Hybrid | 2 PM – 11 PM Shift
Qualification: Bachelor’s Degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Clinical Research, Business Administration, or a related discipline
Experience: Relevant experience in Clinical Operations, Clinical Trial Support, Site Contracts, Clinical Administration, or related functions
Location: Hyderabad, India
Work Mode: Hybrid
Shift: 2:00 PM – 11:00 PM IST
Employment Type: Full-Time
Department: Clinical Operations / Clinical Solutions
Application Mode: Online
🎓 Eligibility Criteria
Applicants should possess:
• Bachelor’s Degree in Life Sciences.
• Pharmacy.
• Nursing.
• Biotechnology.
• Clinical Research.
• Business Administration.
• Or another related discipline.
Candidates with relevant experience in Clinical Operations, Clinical Trial Support, Site Contracts, Clinical Administration, or project coordination are encouraged to
🌟 Why Join Syneos Health?
• Opportunity to work with one of the world’s leading global CROs.
• Hybrid work model with international project exposure.
• Career development through structured learning and mentorship.
• Access to technical and therapeutic area training.
• Collaborative and inclusive workplace culture.
• Work on global clinical trials supporting innovative therapies.
• Exposure to AI-enabled operational tools and modern clinical technologies.
• Career growth across multiple clinical operations functions.
🎯 Key Responsibilities
- ✓ Provide administrative and operational support for clinical projects.
- ✓ Coordinate project documentation and communications across study teams.
- ✓ Maintain shared mailboxes and organize project files.
- ✓ Track project action items and follow up with cross-functional stakeholders.
- ✓ Enter, maintain, and reconcile information in clinical tracking systems.
- ✓ Monitor project timelines, milestones, and potential risks.
- ✓ Assist in contingency planning to minimize project delays.
- ✓ Create, compile, format, version-control, and quality-check clinical documents.
- ✓ Coordinate document translations using approved vendors and systems.
- ✓ Support internal audits and regulatory inspections.
- ✓ Utilize AI-enabled tools, dashboards, and automated reports for operational support.
- ✓ Maintain Trial Master File (TMF) documentation to ensure inspection readiness.
- ✓ Train and mentor junior Clinical Operations Associates when required.
- ✓ Deliver quality outputs while complying with SOPs, Work Instructions, and project requirements.
- ✓ Monitor project workload, timelines, and budgeted hours, escalating issues when necessary.
- ✓ Complete assigned training and maintain compliance records.
💡 Required Qualifications & Skills
Frequently Asked Questions
1. What position is Syneos Health hiring for?
Syneos Health is hiring for the Clinical Support Specialist – Site Contracts Dedicated position.
2. Where is the job located?
The role is based in Hyderabad, India, with a hybrid work model.
3. What are the working hours?
The shift timing is 2:00 PM to 11:00 PM IST.
4. What educational qualifications are preferred?
Candidates with degrees in Life Sciences, Pharmacy, Nursing, Biotechnology, Clinical Research, Business Administration, or related disciplines are encouraged to apply.
5. What are the key responsibilities of this role?
Responsibilities include project coordination, document management, TMF support, timeline tracking, quality control, audit support, and maintaining clinical trial documentation.
6. Is experience with Trial Master File (TMF) important?
Yes. Knowledge of TMF management and inspection-ready documentation is considered an advantage.
7. Will the role involve collaboration with global teams?
Yes. The position requires regular interaction with cross-functional stakeholders involved in global clinical studies.
8. What skills are important for success in this role?
Strong organizational abilities, document management, communication skills, project coordination, SOP compliance, quality control, and attention to detail.
9. Does Syneos Health provide career development opportunities?
Yes. Employees have access to structured training, mentorship, technical learning programs, and long-term career progression opportunities.
10. Why should candidates consider this opportunity?
The role offers hybrid working, exposure to international clinical trials, experience with global clinical operations, and career growth within one of the world’s leading Clinical Research Organizations (CROs).
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