Syneos Health is hiring for two positions: Medical Scientist and Medical Specialist in India. These are full-time, office-based opportunities within the company’s Clinical Solutions team.
The Medical Scientist role is available in Gurugram and Hyderabad, while the Medical Specialist position is based in Gurugram. Candidates with relevant backgrounds in healthcare, biological sciences, clinical research, and medical data review can explore these opportunities.
Job Details
| Particulars | Details |
|---|---|
| Company | Syneos Health |
| Job Category | Clinical Research / Medical Management |
| Job Type | Full-time |
| Work Mode | Office-based |
| Job Location | Gurugram, Hyderabad |
| Job Openings | 2 Positions |
| Posted Date | November 3, 2026 |
1. Medical Scientist
Hiring
Job Requisition ID: 25113976
Job Locations:
- Gurugram, Haryana
- Hyderabad, Telangana
Job Responsibilities
- Work with the Medical Director to develop Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans.
- Coordinate with external medical experts and consultants to obtain scientific and medical inputs.
- Perform regular and ad-hoc medical reviews of data listings and visualizations.
- Analyze clinical data to identify risks, patterns, and trends.
- Prepare medical data queries, review responses, and approve query closures in coordination with the Medical Director.
- Assist with patient profile reviews, scientific data reviews, and protocol deviation reviews.
- Support the preparation of Medical Review Summary reports.
- Participate in medical data review and safety review meetings.
- Prepare presentation slides and support project meetings.
- Coordinate with Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management teams.
- Monitor project deliverables, quality, timelines, and milestones.
- Participate in internal and external audits when required.
- Follow ICH, GCP, data privacy guidelines, and applicable company SOPs.
2. Medical Specialist
Hiring
Job Requisition ID: 25114000
Job Location: Gurugram, Haryana
Job Responsibilities
- Perform Trial Master File (TMF) filing of study-specific medical documents and medical communications.
- Participate in TMF file audits when required.
- Assist Medical Management and Scientific Services teams with eligibility review activities.
- Support the preparation of eligibility review forms and study-related documents.
- Assist with medical review query management and medical data review activities.
- Manage shared mailboxes and route correspondence appropriately.
- Coordinate medical management project meetings.
- Prepare meeting minutes and action items.
- Maintain study-related documentation.
- Upload and manage eligibility review documents in TrialEAS™ and other supporting systems.
- Follow ICH, GCP, data privacy guidelines, company SOPs, and project requirements.
Eligibility Criteria and Qualifications
Medical Scientist
The supplied job description does not list specific educational qualifications or mandatory years of experience for this position.
Candidates should review the responsibilities and assess their experience in medical data review, clinical research, medical management, and cross-functional clinical trial operations.
Medical Specialist
Educational Qualification:
- Postgraduate degree in Biological Sciences.
- Postgraduate degree in a related Natural Sciences or Healthcare discipline.
- Nursing degree.
- Equivalent combination of education and experience.
Experience:
- Solid office or administrative experience.
- 1–2 years of clinical research experience, such as Clinical Trial Assistant (CTA) or Study Coordinator, is preferred but not mandatory.
Required Skills
Medical Scientist
- Medical data review and analysis.
- Clinical data interpretation.
- Medical query management.
- Knowledge of clinical trial protocols.
- Disease-related terminology and pathology.
- Clinical research and drug development knowledge.
- Cross-functional team coordination.
- Project management and documentation.
- ICH-GCP compliance.
Medical Specialist
- Trial Master File (TMF) documentation and filing.
- Medical document management.
- Eligibility review support.
- Clinical research documentation.
- Microsoft Word, Excel, and PowerPoint proficiency.
- Meeting coordination and preparation of minutes.
- Strong written and verbal communication.
- Organizational and multitasking skills.
- Attention to detail and deadline management.
- Knowledge of medical terminology and drug development processes.
