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Clinical Support Specialist - Site Contracts Dedicated (2 Pm To 11 Pm Shift- Hyderabad- Hybrid)

Syneos Health
1-3 years
₹5 LPA – ₹8 LPA
Hyderabad, Remote, India, India
15 July 8, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Clinical Support Specialist – Site Contracts Dedicated (2 PM – 11 PM Shift)

Company: Syneos Health
Location: Hyderabad, India (Hybrid)
Job ID: 25110008
Updated On: July 6, 2026
Shift Timing: 2:00 PM – 11:00 PM


Job Summary

Syneos Health is hiring a Clinical Support Specialist – Site Contracts Dedicated to provide operational and administrative support for clinical research projects. The role involves managing project documentation, maintaining clinical tracking systems, supporting Trial Master File (TMF) activities, coordinating with cross-functional teams, and ensuring high-quality project delivery while maintaining compliance with clinical research standards.


Key Responsibilities

  • Coordinate project documentation and maintain shared mailboxes.

  • Organize project files and track action items.

  • Maintain and reconcile data in clinical and project tracking systems.

  • Track project timelines, milestones, and identify potential risks.

  • Investigate delays and support contingency planning.

  • Create, compile, format, version-control, and QC project documents.

  • Coordinate document translations through approved vendors.

  • Support audits and regulatory inspections.

  • Utilize AI-enabled tools, dashboards, and reports for operational support.

  • Assist with Trial Master File (TMF) documentation and filing.

  • Train and mentor junior Clinical Operations Associates.

  • Ensure compliance with SOPs, Work Instructions, and project requirements.

  • Monitor workload, project hours, and budget utilization.

  • Complete mandatory training and maintain accurate timesheets.

  • Support overall clinical operations and project coordination.


Required Skills

  • Clinical Operations

  • Clinical Research Documentation

  • Trial Master File (TMF)

  • Project Coordination

  • Document Management

  • Timeline & Milestone Tracking

  • Risk Assessment

  • Quality Control (QC)

  • SOP & GCP Compliance

  • AI-enabled Reporting Tools

  • Microsoft Office Suite

  • Communication & Coordination

  • Attention to Detail

  • Time Management


Eligibility

  • Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a related field.

  • Experience in clinical research, clinical operations, or project coordination is preferred.

  • Knowledge of GCP, TMF, and clinical documentation processes is an advantage.

  • Good communication and organizational skills.


Experience

Preferred Experience: 1–3 years of experience in Clinical Operations, Clinical Research, Site Contracts, TMF Management, or Clinical Project Support.


Salary Package (Estimated Market Standard)

₹5 LPA – ₹8 LPA (depending on experience, skills, and interview performance).


Work Mode

  • Hybrid

  • Hyderabad Location

  • Evening Shift (2 PM – 11 PM)


Why Join Syneos Health?

  • Career growth and learning opportunities.

  • Global exposure to clinical research projects.

  • Inclusive and collaborative work culture.

  • Technical and therapeutic area training.

  • Employee recognition and rewards programs.

  • Opportunity to work on global clinical trials and innovative healthcare solutions.


About Syneos Health

Syneos Health is a leading global life sciences organization that supports pharmaceutical, biotechnology, and healthcare companies throughout the drug development and commercialization process. Over the past five years, the company has contributed to 94% of FDA-approved novel drugs, 95% of EMA-authorized products, and managed 200+ studies across 73,000 sites with over 675,000 clinical trial participants.