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Medical Writer I (Junior Project Specialist – 1 Year Contract)

Syneos Health
1+ years
INR 4 LPA – 7 LPA
Gurgaon, Remote, India, India
1 July 2, 2026
Job Description
Job Type: Contract Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Basic Statistics Interpretation, Clinical Research Knowledge, Evidence Synthesis, Literature Review, Medical Writing, MS Word, Narrative Writing, Scientific Writing

Medical Writer I (Junior Project Specialist – 1 Year Contract)

Company: Syneos Health
Location: Remote (India) / Gurugram (Hybrid)
Department: Medical Writing / Clinical Operations
Job Type: Full-Time (1-Year Contract)


JOB OVERVIEW

The Medical Writer I (Junior Project Specialist) is responsible for supporting medical writing and document management activities by ensuring accurate filing, organization, and maintenance of clinical and regulatory documents within Veeva RIM/eTMF systems. The role focuses on document quality, regulatory compliance, metadata management, electronic archiving, and adherence to GxP, FDA, and EU guidelines while collaborating with cross-functional teams to support clinical development projects.


KEY RESPONSIBILITIES

Document Management

  • Perform document filing within Veeva RIM.

  • Upload and organize documents in Veeva eTMF.

  • Download records from internal systems.

  • Ensure accurate document classification and storage.

  • Maintain document version control.

  • Organize project documentation systematically.

  • Ensure secure electronic document archiving.

eTMF Management

  • Perform eTMF filing activities.

  • Support Trial Master File (TMF) management.

  • Maintain complete and accurate TMF documentation.

  • Validate filing accuracy.

  • Ensure timely filing of project documents.

  • Maintain inspection-ready documentation.

Quality & Compliance

  • Ensure document quality before filing.

  • Verify document integrity.

  • Follow GxP guidelines.

  • Maintain compliance with FDA regulations.

  • Adhere to EU regulatory guidelines.

  • Follow sponsor-specific requirements.

  • Support regulatory inspection readiness.

Metadata & Filing

  • Apply correct document naming conventions.

  • Validate metadata accuracy.

  • Assign appropriate document classifications.

  • Store documents in correct Veeva locations.

  • Improve document retrieval efficiency.

Project Support

  • Track project documentation.

  • Maintain project timelines.

  • Monitor filing milestones.

  • Update project status regularly.

  • Notify project leads of delivery risks.

  • Support multiple concurrent projects.

Clinical Documentation

  • Support Early Access Program documentation.

  • Manage External Research Project documents.

  • Handle Observational Study documentation.

  • Support Non-Interventional Study documentation.

  • Maintain regulatory filing records.

Process Improvement

  • Contribute to SOP development.

  • Support workflow improvements.

  • Adapt to new operational processes.

  • Assist in refining filing procedures.

  • Promote best practices in document management.

Cross-Functional Collaboration

  • Collaborate with client stakeholders.

  • Participate in internal meetings.

  • Attend client-facing meetings.

  • Resolve document-related comments.

  • Support communication across project teams.

Regulatory Compliance

  • Maintain knowledge of FDA requirements.

  • Follow EU regulatory guidance.

  • Ensure compliance with industry standards.

  • Maintain sponsor-specific compliance requirements.


EDUCATIONAL QUALIFICATIONS

  • Bachelor's Degree in:

    • Pharmacy

    • Life Sciences

    • Biotechnology

    • Biology

    • Biomedical Sciences

    • Medicine

    • Related Scientific Discipline

Preferred

  • Master's Degree in Life Sciences or related field.


EXPERIENCE REQUIREMENTS

Required

  • Experience with document management systems is preferred.

  • Familiarity with Veeva RIM/eTMF is an advantage.

  • Basic understanding of GxP guidelines.

  • Knowledge of clinical and regulatory documentation.

  • Good written and verbal communication skills.

  • Strong attention to detail.

Preferred

  • Experience with Veeva Vault.

  • Exposure to Clinical Trials documentation.

  • Knowledge of FDA and EU regulations.