Medical Writer Clinical Trial Transparency Remote Job Syneos Health, registry submissions, and global disclosure databases in remote work model.
About the Company
Syneos Health is a leading global biopharmaceutical solutions organization providing integrated clinical development, commercialization, and consulting services to pharmaceutical, biotechnology, and medical device companies. With a strong presence across regulated markets, Syneos Health supports sponsors throughout the entire product lifecycle, from early development to post-marketing activities.
The organization is widely recognized for its expertise in clinical research, regulatory compliance, medical writing, and clinical trial transparency. Syneos Health works closely with global regulatory authorities and clinical trial registries to ensure accurate, timely, and compliant disclosure of clinical trial information.
Employees at Syneos Health benefit from exposure to international regulations, global study portfolios, and structured career development in a collaborative and compliance-driven environment. Medical Writer Clinical Trial Transparency
Job Details
- Job Title: Medical Writer – Clinical Trial Transparency (CTT / Disclosure)
- Company: Syneos Health
- Job Type: Full-Time
- Work Mode: Remote / Home Based
- Job Location: India (Remote)
- Experience Required: 1 to 3 years
- Education Required: Bachelor’s or Master’s degree
- Industry: Clinical Research / Medical Writing / Regulatory Disclosure
- Application Mode: Online Application / Email Application
- Job Status: Verified Job
Job Description
Syneos Health is inviting applications for the role of Medical Writer – Clinical Trial Transparency (CTT / Disclosure). This is a fully remote opportunity designed for early-career medical writers with hands-on experience in clinical trial disclosure, transparency regulations, and registry submissions. Medical Writer Clinical Trial Transparency
The role focuses on ensuring accurate and compliant registration and results reporting of clinical trials across global registries. Selected candidates will work on disclosure activities throughout the clinical trial lifecycle and gain specialized expertise in transparency regulations across multiple regions.
This position is an excellent entry point for professionals seeking long-term growth in clinical trial transparency, regulatory disclosure, and global compliance. Medical Writer Clinical Trial Transparency
Key Responsibilities
As a Medical Writer – Clinical Trial Transparency, the selected candidate will be responsible for the following activities:
- Prepare, review, and submit clinical trial disclosure documentation in compliance with global transparency regulations
- Manage protocol registration and results disclosure on global clinical trial registries, including:
- ClinicalTrials.gov (CT.gov)
- Clinical Trial Information System (CTIS) under EU CTR
- EudraCT
- Support clinical trial transparency activities across the entire study lifecycle
- Ensure timely and accurate updates to registry records based on protocol amendments and study milestones
- Work with disclosure databases such as PharmaCM, Disclose, or similar transparency systems
- Maintain consistency, accuracy, and regulatory compliance of all submitted trial information
- Collaborate with cross-functional teams including Clinical Operations, Regulatory Affairs, Medical Affairs, and Project Management
- Track disclosure timelines and maintain audit-ready documentation
- Support internal and external audits related to transparency and disclosure compliance
- Address comments, queries, and follow-up requests from registry authorities
Medical Writer Clinical Trial Transparency
Skills / Qualifications
Educational Qualifications
- Bachelor’s degree in Pharmacy, Life Sciences, or Biomedical Sciences
- Master’s degree in Pharmacy, Life Sciences, or Biomedical Sciences
Experience Requirements
- 1 to 3 years of experience in Medical Writing or Clinical Trial Transparency
- Mandatory hands-on experience in clinical trial disclosure and transparency activities
Technical & Professional Skills
- Strong working knowledge of clinical research processes
- Practical experience with global clinical trial registries such as:
- ClinicalTrials.gov
- CTIS (EU CTR)
- EudraCT
- Understanding of protocol registration and results disclosure workflows
- Experience using disclosure databases such as PharmaCM, Disclose, or similar platforms
- Excellent written communication and regulatory writing skills
- High attention to detail and ability to manage compliance-driven documentation
- Strong organizational and time management skills
Medical Writer Clinical Trial Transparency
Salary & Compensation
- Estimated Salary Range: ₹6,00,000 to ₹10,00,000 per annum
- Compensation will be based on experience, skills, and internal assessment
- Competitive salary aligned with industry standards
Medical Writer Clinical Trial Transparency
Benefits / Perks
- 100% remote / work-from-home opportunity
- Exposure to global clinical trial transparency regulations
- Structured career development in medical writing and regulatory disclosure
- Opportunity to work with a leading global CRO and biopharma partner
- Collaborative and compliance-focused work environment
- Long-term career stability and skill specialization
Medical Writer Clinical Trial Transparency
Why You Should Join
Joining Syneos Health as a Medical Writer – Clinical Trial Transparency provides a unique opportunity to specialize in one of the most critical and growing areas of clinical research compliance. This role enables professionals to gain in-depth exposure to global transparency regulations, international registries, and regulatory expectations. Medical Writer Clinical Trial Transparency
Employees benefit from working on global studies, learning from experienced transparency professionals, and building a strong foundation in disclosure and compliance. The remote work model further supports work-life balance while contributing to meaningful regulatory activities that ensure ethical and transparent clinical research. Medical Writer Clinical Trial Transparency Medical Writer Clinical Trial Transparency
FAQs
Who can apply for this Medical Writer – CTT role?
Candidates with 1–3 years of experience in medical writing or clinical trial transparency and relevant life sciences qualifications can apply.
Is this a remote role?
Yes. This is a fully remote, home-based position within India.
Is clinical trial disclosure experience mandatory?
Yes. Hands-on experience in clinical trial transparency and registry submissions is mandatory.
Which registries will I work on?
You will work on ClinicalTrials.gov, CTIS (EU CTR), and EudraCT.
Is this role suitable for early-career professionals?
Yes. This role is ideal for early-career medical writers looking to specialize in clinical trial transparency.
How to Apply
Interested and eligible candidates can apply through one of the following options:
Online Application: Apply through the official Syneos Health career portal
Email Application:
Send your updated CV to anamika.jayprakash@syneoshealth.com
Applicants are advised to highlight their experience with clinical trial registries, disclosure databases, and transparency activities to improve shortlisting chances.
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
