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Principal Medical Writer (Ctt)

8+ years
Not Disclosed
10 April 3, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

 


 


Principal Medical Writer (CTT)

Company: Syneos Health
Location: India
Experience: 8+ years

About Syneos Health

Syneos Health is a global biopharmaceutical solutions leader with 25,000+ employees committed to accelerating drug development. By working with 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products in the past five years, we have helped transform lives through innovation.

Join us—because work here matters everywhere.


Job Summary

The Principal Medical Writer (CTT) will be responsible for clinical trial disclosure (CTT), redaction, and anonymization of clinical documents for regulatory submissions. This role involves authoring, reviewing, and quality assurance of critical trial-related documents to ensure global compliance (EMA Policy 0070, Health Canada PRCI, EUCTR, NIH Final Rule, DIMDI).


Key Responsibilities

Clinical Trial Disclosure & Regulatory Compliance

  • Author, redact, and review clinical trial disclosure documents, including:

    • Clinical Study Reports (CSRs)

    • Patient Narratives

    • Clinical Summaries

    • Protocol and Results Summaries for regulatory submissions

  • Ensure compliance with regulations across global agencies (EMA, Health Canada, NIH, EUCTR, DIMDI).

  • Perform quality control (QC) checks on documents per standard operating procedures (SOPs).

  • Work with clinical trial disclosure databases (e.g., Disclose, Prime, PRS, EudraCT).

Quality Assurance & Client Interaction

  • Review and edit documents to maintain high-quality standards.

  • Communicate effectively with internal teams and external stakeholders.

  • Ensure adherence to client-specific disclosure processes.

Training & Leadership

  • Mentor and train junior medical writers on clinical trial transparency and regulatory guidelines.

  • Participate in internal and client-specific training programs.


Qualifications & Skills

Education & Experience

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.

  • 8+ years of experience in medical writing, clinical trial disclosure, and regulatory submissions.

Technical & Regulatory Knowledge

  • Strong understanding of clinical trial transparency fundamentals.

  • Knowledge of clinical development, ICH-GCP guidelines, and regulatory requirements.

  • Experience with clinical trial registries (e.g., ClinicalTrials.gov).

  • Proficiency in Microsoft Word, Excel, PowerPoint, and CTT databases (Disclose, Prime, PRS, EudraCT).

Soft Skills

  • Strong analytical skills to interpret scientific and regulatory information.

  • Excellent written and verbal communication for high-quality document review.

  • Ability to lead and mentor teams while working in a collaborative environment.

  • High attention to detail and ability to manage multiple projects.


Why Join Syneos Health?

  • Worked on 94% of all Novel FDA-Approved Drugs in the past five years.

  • Collaborated on 95% of EMA-Authorized Products and 200+ studies across 73,000 sites.

  • Competitive career growth, mentorship, and rewards program.

  • Be part of a diverse, inclusive, and innovative workplace.


Join Us

If you have relevant experience, apply now or join our Talent Network for future opportunities at Syneos Health.

 

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