Syneos Health is hiring a Medical Writer I (Junior Project Specialist) for a 1-year contract role. This is an excellent opportunity for candidates with strong regulatory document knowledge and Veeva RIM/eTMF experience seeking medical writer jobs, clinical research, or regulatory affairs positions in India. Both remote (pre-approved) and hybrid options in Gurugram are available.
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About the Company
Syneos Health is a leading fully integrated biopharmaceutical solutions organization that combines clinical and commercial expertise to accelerate customer success. With a global presence, Syneos Health partners with pharmaceutical and biotech companies across drug development and commercialization.
The company is known for its strong focus on innovation, employee development, inclusive culture, and delivering high-impact solutions that advance patient care.
Job Details
- Company Name: Syneos Health
- Position: Medical Writer I (Junior Project Specialist)
- Duration: 1 Year Contract
- Experience: Junior level (0–3 years preferred with relevant exposure)
- Qualification: Bachelor’s / Master’s degree in Life Sciences, Pharmacy, or related field
- Location: Remote (Pre-Approved) or Hybrid – Gurugram, Haryana
- Work Type: Full-time
Job Description
Syneos Health is looking for a detail-oriented and proactive Medical Writer I to support document management and regulatory filing activities. The role primarily involves working within Veeva RIM and eTMF systems to ensure accurate, compliant, and timely document handling for clinical and regulatory projects.
Medical Writer I (Junior Project Specialist)
- Department: Medical Writing / Clinical Solutions
- Role: Junior Project Specialist
- Employment Type: 1 Year Contract
- Location: Remote or Hybrid (Gurugram)
- Experience: Suitable for candidates with strong GxP and document management understanding
Skills/Qualifications
- Good understanding of GxP guidelines and regulatory requirements (FDA, EU)
- Working knowledge of Veeva RIM and eTMF systems
- Strong attention to detail and document quality control
- Excellent organizational and time management skills
- Good communication and collaboration abilities
- Familiarity with ICH guidelines and clinical trial documentation
- Experience in digital archiving and metadata management is a plus
Key Responsibilities
- Perform document filing and management in Veeva RIM and eTMF
- Download, classify, and upload documents with accurate metadata
- Ensure documents meet quality, integrity, and compliance standards
- Support ICH stability studies and regulatory submissions
- Maintain project tracking and meet delivery timelines
- Contribute to SOP creation and process improvements
- Collaborate with client stakeholders and project teams
- Participate in internal and client-facing meetings
Benefits/Perks
- Opportunity to work with a global leader in biopharmaceutical solutions
- Exposure to international regulatory standards and Veeva platforms
- Flexible remote/hybrid working options
- Strong focus on career development and learning
- Inclusive and collaborative work culture
- Competitive contract compensation
How to Apply
Interested candidates can apply directly through the Syneos Health career portal using Job Requisition ID: 25108568. For more medical writing jobs, clinical research, and regulatory affairs opportunities across India, visit Pharma Recruiter.
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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Syneos Health Career page.
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Why You Should Join
Syneos Health offers a dynamic environment where you can build a strong foundation in medical writing and regulatory document management. With exposure to global projects and advanced tools like Veeva, this role provides excellent learning and growth potential in the life sciences industry while contributing to solutions that impact patient lives.
FAQs
What is the duration of the Medical Writer I position?
This is a 1-year contract role with possibility of extension.
Is the job fully remote?
It is Remote (Pre-Approved) or Hybrid in Gurugram.
What experience is required?
Suitable for junior candidates with strong understanding of GxP, document management, and regulatory filing.
Which systems will I work on?
Primarily Veeva RIM and eTMF for document filing and management.
This contract opportunity at Syneos Health is ideal for professionals looking to start or grow their career in medical writing and clinical regulatory operations. Apply soon using Job ID 25108568.
