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Hiring Now: Clinical Trial Assistant & Sr. Medical Editor at Syneos Health

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Syneos Health

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Medicine, Ph.D

Mumbai & remote

3 Years+

Verified Job

Online Application
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Syneos Health, a leading global clinical research organization, is inviting experienced professionals to join their growing teams in Clinical Operations and Medical Editing. These roles offer the opportunity to work on innovative global studies and regulatory documentation for top pharmaceutical clients.

If you have hands-on experience in clinical trial management, TMF documentation, or medical editing for regulatory documents, this could be your ideal career move.


🧬 Open Positions

🔹 1. Senior Clinical Trial Assistant (Sr. CTA) / Clinical Trial Assistant (CTA)

Location: Mumbai (Hybrid)
Department: Clinical Operations

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Key Responsibilities

  • Handle investigator site queries and maintain Trial Master File (TMF) documentation.
  • Coordinate invoice and grant payments, ensuring accurate tracking and processing.
  • Support ethics committee submissions and regulatory dossier submissions.
  • Prepare Site Initiation Visit (SIV) packages and manage study supplies.
  • Collaborate closely with project teams for Phase IV clinical studies.

Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related discipline.
  • Minimum 3 years of experience in clinical operations.
  • Strong understanding of GCP, ICH guidelines, and clinical trial documentation.
  • Excellent organizational and communication skills.

🔹 2. Senior Medical Editor

Location: Remote (Home-Based)
Department: Medical Writing / Regulatory Affairs

Key Responsibilities

  • Edit and format regulatory documents including protocols (mandatory), Clinical Study Reports (CSR), and Investigator’s Brochures (IB).
  • Ensure compliance with client and regulatory requirements for style and structure.
  • Lead project management activities and coordinate with internal and client teams.
  • Provide editorial oversight for accuracy, consistency, and adherence to timelines.

Qualifications

  • Minimum 3+ years of relevant experience in medical editing and regulatory writing.
  • Proven project management and client-facing experience.
  • Excellent English language and grammar proficiency.
  • Strong attention to detail and ability to manage multiple deliverables.

💼 Why Join Syneos Health?

  • Work with a global leader in clinical research and biopharmaceutical solutions.
  • Hybrid and remote opportunities for flexibility.
  • Exposure to international studies and regulatory submissions.
  • Competitive compensation and professional growth opportunities.

📩 How to Apply

Interested candidates can apply through the official links below:

Alternatively, send your CV directly to:
📧 anamika.jayprakash@syneoshealth.com

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