Syneos Health Hiring for Clinical Document Agent | 1–3 Years | Remote
Syneos Health is hiring for the position of Clinical Document Agent for its Research & Development team. The role offers a remote work opportunity, with the hiring office located in Hyderabad.
The position is suitable for candidates with experience in clinical trial documentation, Phase 1 clinical trials, Investigator Site Files (ISF), document quality control, Excel-based documentation, and Adobe tools.
Job Details
| Details | Information |
|---|---|
| Company | Syneos Health |
| Position | Clinical Document Agent |
| Experience | 1–3 Years |
| Work Mode | Remote |
| Hiring Office | Hyderabad |
| Openings | 2 |
| Employment Type | Full Time, Permanent |
| Department | Research & Development |
| Industry | Pharmaceutical & Life Sciences |
Key Responsibilities
- Manage and maintain clinical trial documentation.
- Apply knowledge of Phase 1 clinical trial documentation.
- Work with Investigator Site Files (ISF) and related documentation.
- Perform document quality control (QC) activities.
- Create forms and source documentation using Microsoft Excel.
- Use Excel to develop and manage clinical documentation.
- Work with Adobe and other computer-based documentation tools.
- Understand project requirements and translate them into appropriate documentation.
- Coordinate with cross-functional and global teams.
- Communicate effectively with stakeholders involved in clinical documentation activities.
Required Skills
Candidates should have experience or knowledge in:
- Clinical Trial Documentation
- Phase 1 Clinical Trials
- Investigator Site Files (ISF)
- Document Quality Control
- Microsoft Excel
- Form & Source Documentation Creation
- Adobe
- Clinical Research
- Cross-functional Coordination
- Global Team Collaboration
- Communication Skills
Educational Qualification
Undergraduate:
- B.Sc. in any specialization
- B.Pharm in any specialization
Postgraduate:
- M.Sc./MS in Science
- M.Pharm
Who Can Apply?
Candidates with 1–3 years of relevant experience in clinical documentation, clinical research, or related pharmaceutical/life sciences functions can consider this opportunity.
Experience with Phase 1 clinical trials and document QC is specifically required for the role.
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