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Principal Medical Writer (Ctt)

0-2 years
Not Disclosed
10 March 31, 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)

๐Ÿ“ Location: India-Asia Pacific - IND-Home-Based
๐Ÿ“Œ Job ID: 25002335
๐Ÿ“… Updated: March 27, 2025

About Syneos Health

Syneos Health® is a leading biopharmaceutical solutions organization, dedicated to accelerating drug development and market success. With 25,000+ employees worldwide, we provide clinical and commercial solutions to bring life-changing therapies to patients faster.

Job Overview

As a Principal Medical Writer (Clinical Trial Transparency - CTT), you will be responsible for authoring, reviewing, and quality-checking clinical trial disclosure documents. You will ensure compliance with global regulatory requirements (EMA Policy 0070, Health Canada PRCI, EUCTR, NIH Final Rule, and national registries like DIMDI) while supporting clinical trial transparency initiatives.

Key Responsibilities

Clinical Trial Disclosure & Medical Writing

โœ” Author and quality-check clinical study documents (e.g., clinical study reports, patient narratives, clinical summaries).
โœ” Prepare disclosure documents (e.g., Protocol Registration Form and Result Registration Form) for ClinicalTrials.gov and other registries.
โœ” Ensure compliance with global regulatory guidelines (EMA Policy 0070, Health Canada PRCI, EUCTR, NIH Final Rule).
โœ” Perform redaction/anonymization of clinical documents for regulatory submission.

Quality Assurance & Compliance

โœ” Conduct quality control (QC) reviews of documents based on pre-specified checklists.
โœ” Ensure adherence to client-specific processes and regulatory standards.
โœ” Maintain detailed documentation and audit readiness.

Project Coordination & Client Interaction

โœ” Collaborate with cross-functional teams (clinical, regulatory, and biostatistics teams).
โœ” Communicate effectively with clients and regulatory authorities regarding document requirements.
โœ” Participate in internal and external project meetings as required.

Training & Mentorship

โœ” Provide training and mentorship to junior medical writers.
โœ” Stay updated on industry trends, regulatory changes, and best practices in clinical trial disclosure.

Qualifications & Skills

๐ŸŽ“ Education:
๐Ÿ”น Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or a related field.

๐Ÿ’ก Experience & Technical Skills:
โœ” 8+ years of medical writing experience in clinical trial transparency (CTT), redaction, and anonymization.
โœ” Strong knowledge of global regulatory requirements (EMA, FDA, Health Canada, NIH, EUCTR, national registries).
โœ” Experience with CTT databases (Disclose, Prime, PRS, EudraCT) is a plus.
โœ” Proficiency in Microsoft Word, Excel, PowerPoint.

๐Ÿ—ฃ Soft Skills:
โœ” Strong analytical skills and attention to detail.
โœ” Excellent written and verbal communication skills.
โœ” Ability to work in a fast-paced, deadline-driven environment.
โœ” Proactive, adaptable, and a strong team player.

Why Join Syneos Health?

๐Ÿ”น Work on 94% of FDA-approved drugs in the past five years.
๐Ÿ”น Career growth with technical training, mentorship, and leadership opportunities.
๐Ÿ”น Collaborative and innovative Total Self culture that values diversity and inclusion.

๐Ÿ’ผ Apply Today!
Join Syneos Health and contribute to global clinical trial transparency efforts.