WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now

Clinical Trial Disclosure Writer Role at Syneos Health – Hiring Now

Published on

Syneos Health

B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences, Ph.D., MBBS, BDS, BHMS, BAMS, Postgraduate Diploma in Clinical Research, Postgraduate Diploma in Medical Writing

Remote

6 Months - 1 Years

Verified Job

Email Application
Advertisement

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, accelerating customer success through clinical, medical affairs, and commercial expertise. With 29,000 employees across 110 countries, Syneos Health has supported 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products in the last five years.

Advertisement

The company fosters a Total Self culture, emphasizing diversity, inclusion, and career growth, making it a top workplace in the pharma industry.

Detailed Job Description

Job Title: Medical Writer I (CTT)

Location: Pune, India
Job ID: 25000363
Updated: Recently

Key Responsibilities:

  • Serve as a medical writer for clinical study/regulatory projects.
  • Assist in writing, editing, and coordinating clinical/regulatory documents.
  • Work on Clinical Trial Disclosures (CTT), including protocol registration and results posting for regulatory bodies.
  • Prepare and review:
    • Clinical study protocols & amendments
    • Clinical study reports (CSRs)
    • Patient narratives
    • Investigator brochures
  • Ensure compliance with ICH-E3 guidelines and client-specific standards.
  • Collaborate with data management, biostatistics, and regulatory teams.
  • Perform literature searches and stay updated with regulatory guidelines.

Eligibility Criteria:

  • Minimum 6 months to 1 year of experience in Clinical Trial Disclosure (CTT) or related medical writing.
  • B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences, Ph.D. in Life Sciences, Ph.D. in Pharmacy, Ph.D. in Medical Sciences, MBBS, BDS, BHMS, BAMS, Postgraduate Diploma in Clinical Research, Postgraduate Diploma in Medical Writing
  • Experience in protocol registration, results registration, and regulatory submissions.
  • Strong understanding of clinical research documentation and statistical analysis plans.
  • Excellent scientific writing, editing, and communication skills.
  • Ability to work under moderate supervision and meet deadlines.

Benefits & Why Join Syneos Health?

✅ Career Growth: Professional development in medical writing & regulatory affairs.
✅ Global Impact: Work on cutting-edge clinical trials with top biopharma clients.
✅ Inclusive Culture: Emphasis on diversity, equity, and work-life balance.
✅ Learning Opportunities: Access to technical & therapeutic training programs.
✅ Competitive Compensation: Attractive salary & benefits package.

Advertisement

How to Apply

📩 Apply Now: Send your CV to vishal.milindkulkarni@syneoshealth.com

Clinical Trial Disclosure Writer Role at Syneos Health – Hiring Now
Advertisement

Share This Job

✅ Job Copied Successfully!

PharmaBharat Editorial Team

The PharmaBharat Editorial Team, comprised of pharmaceutical industry experts with over 3 years of collective experience in research, regulatory affairs, and market analysis, delivers accurate and timely updates on trends, innovations, and career opportunities. Our content is rigorously vetted by professionals with advanced degrees in pharmacy and biotechnology, ensuring authoritative and trustworthy insights for job seekers in the pharmaceutical sector.

Ad Popup