Syneos Health hiring Medical Writer I

Medical Writer Jobs for M.Pharm & Pharm.D in Gurugram | Syneos Health Hiring

 Syneos Health hiring Medical Writer I in Gurugram. Vacancies for M.Pharm, Pharm.D postgraduates with experience in regulatory writing. Apply now.

Join Syneos Health as a Medical Writer I in Gurugram (Hybrid Role)

Looking to grow your medical writing career with a global biopharmaceutical solutions company? Syneos Health is actively hiring Medical Writer I professionals in Gurugram, India for its hybrid work model. Candidates with M.Pharm, Pharm.D, or life sciences postgraduate degrees and relevant experience in regulatory medical writing or clinical trial documentation are highly encouraged to apply.

Why Work at Syneos Health?

Syneos Health, a globally integrated biopharmaceutical services provider, works with over 94% of all novel FDA-approved drugs. With a workforce of 29,000 across 110 countries, Syneos offers a robust career development framework, global exposure, and a Total Self culture that supports diversity, authenticity, and personal growth.

Current Opening: Medical Writer I

Key Responsibilities

• Draft, compile, and edit various medical and clinical documents, including:
  • Clinical study protocols and amendments
  • Clinical study reports
  • Patient narratives
  • Investigator brochures
• Conduct statistical review and provide feedback on tables/figures/listings
• Collaborate with teams in data management, biostatistics, regulatory and medical affairs
• Perform online literature searches for clinical data support
• Adhere to ICH-E3 guidelines and company SOPs/templates
• Maintain quality and compliance in deliverables within budget and timeline
• Support quality checks and documentation for regulatory platforms like ClinicalTrials.gov, EUCTR, and US FDA submissions

Educational Qualification & Experience

• Required Education: M.Pharm, Pharm.D, or postgraduate in Life Sciences
• Preferred Background:
  • Experience in regulatory medical writing, pharmacovigilance, or clinical trial disclosure
  • Familiarity with clinical trial documentation and CTD writing
  • Hands-on experience with US FDA, EUCTR, or ct.gov platforms

Work Location

📍 India – Asia Pacific – Gurugram (Hybrid)

This hybrid role provides flexibility to balance office collaboration with remote work opportunities.

Apply Now

Candidates looking to accelerate their regulatory writing career with a world-renowned company should apply here.

🕒 Note: This role may require occasional travel (less than 25%). Immediate joiners preferred.

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