Syneos Health is inviting applications for the position of Medical Writer I (Junior Project Specialist – 1 Year Contract) for remote and hybrid work locations in India. This opportunity is ideal for candidates from life sciences, pharmacy, biotechnology, clinical research, and medical writing backgrounds looking to build a career in regulatory documentation, Veeva systems, eTMF management, and clinical operations.
The company is one of the leading global clinical research and healthcare solutions organizations, supporting drug development and regulatory operations worldwide. Candidates with strong documentation skills, GxP understanding, and interest in medical writing and regulatory workflows are encouraged to apply.
Job Overview
| Details | Information |
|---|---|
| Job Title | Medical Writer I (Junior Project Specialist) |
| Company | Syneos Health |
| Job Type | Full-Time |
| Contract Duration | 1 Year |
| Work Mode | Remote / Hybrid |
| Location | India (Remote) & Gurugram |
| Department | Clinical Solutions |
| Experience | Freshers to Experienced |
| Industry | Clinical Research / Medical Writing / Regulatory Affairs |
Key Responsibilities
The selected candidates will work on medical writing support, document management, regulatory filing, and Veeva-based documentation activities.
Major Responsibilities Include:
- Supporting compliant document filing within Veeva RIM systems
- Managing eTMF filing activities following GxP guidelines
- Uploading and categorizing regulatory and clinical project documents
- Ensuring document quality, integrity, and metadata accuracy
- Maintaining proper naming conventions and electronic archiving standards
- Supporting Early Access Programs, observational studies, and external research projects
- Collaborating with client stakeholders and internal project teams
- Monitoring project timelines and submission deadlines
- Participating in internal and client-facing meetings
- Contributing to SOPs, workflows, and process improvements
- Maintaining compliance with FDA, EMA, and global regulatory standards
Required Qualifications
Candidates with the following educational backgrounds may apply:
- B.Pharm
- M.Pharm
- Pharm.D
- MSc Life Sciences
- Biotechnology
- Biochemistry
- Clinical Research
- Other Healthcare or Life Sciences Degrees
Preferred Skills
- Knowledge of Veeva RIM or eTMF systems
- Understanding of GxP guidelines
- Strong attention to detail
- Documentation and file management skills
- Communication and stakeholder coordination abilities
- Basic understanding of regulatory and clinical documentation
Why Join Syneos Health?
Working at Syneos Health offers exposure to global clinical trials, regulatory projects, and medical writing operations.
Employee Benefits
- Remote work flexibility
- Career growth and professional development
- Training in clinical research and regulatory systems
- Exposure to global pharmaceutical projects
- Inclusive and collaborative work culture
- Opportunity to work with leading healthcare clients worldwide
According to the company, Syneos Health has contributed to:
- 94% of Novel FDA Approved Drugs
- 95% of EMA Authorized Products
- 200+ studies across 73,000+ sites globally
How to Apply
