Remote Syneos Health Hiring Clinical Trial Disclosure / Regulatory Writers
Organization: Syneos Health
Position: Medical Writer – Clinical Trial Disclosure & Regulatory Writing
Experience: 1 – 3 Years
Salary: ₹4 – ₹7 LPA
Location: Work from Home (Remote)
Qualification: M.Pharm, PharmD, or any Life Sciences Postgraduate
Job Type: Full-Time, Permanent
Mode of Application: Online
If you are a postgraduate in Life Sciences with an interest in scientific communication, regulatory documentation, and clinical trial transparency, then this opportunity from Syneos Health can be the ideal starting point for your career as a Medical Writer. Remote Syneos Health Hiring Clinical Trial
This remote job offers the flexibility of working from home along with career advancement in one of the most demanding roles in the pharmaceutical industry.
About Syneos Health
Syneos Health is a leading Contract Research Organization (CRO) that partners with biopharmaceutical companies to accelerate clinical development and commercial delivery of medical innovations. With operations in over 110 countries, Syneos Health provides end-to-end services including clinical trial management, regulatory writing, data analysis, pharmacovigilance, and real-world evidence. Remote Syneos Health Hiring Clinical Trial
The company is known for its commitment to innovation, technology integration, and high-quality standards, making it a trusted employer for thousands of professionals in the healthcare sector globally.
Job Overview – Medical Writer (Remote)
Syneos Health is currently hiring entry-level to mid-level Medical Writers for their Clinical Trial Disclosure and Regulatory Writing division. Selected candidates will be responsible for developing and editing a range of regulatory and clinical trial documents to support drug development activities.
This is a remote, full-time role, suitable for candidates across India who have 1–3 years of experience in medical writing or regulatory documentation. Remote Syneos Health Hiring Clinical Trial
Key Responsibilities
As a Medical Writer, your core responsibilities will include:
- Authoring Clinical Documents: Write and edit critical regulatory documents such as:
- Clinical Study Protocols and Amendments
- Clinical Study Reports (CSRs)
- Investigator Brochures (IBs)
- Patient Narratives
- Disclosure Activities: Prepare content for ClinicalTrials.gov (CT.gov) and EUCTR platforms for clinical trial transparency and regulatory submissions.
- Collaborating with Cross-functional Teams: Work with data management, biostatistics, safety, and regulatory teams to ensure accuracy and consistency in documents.
- Literature Search & Evidence Gathering: Conduct literature reviews to support background and scientific rationale.
- Guideline Adherence: Ensure all documents comply with ICH-E3, GCP, FDA, EMA, and internal SOPs.
- Timeline Management: Work within defined budgets and timelines to deliver high-quality writing assignments.
Candidate Profile
Educational Qualification:
- M.Pharm, PharmD, or Postgraduate in Life Sciences (e.g., MSc in Biotechnology, Microbiology, Pharmacology, etc.)
Experience Required:
- 1 to 3 years of relevant experience in medical writing, clinical trial disclosure, or pharmacovigilance.
- Hands-on experience with:
- CT.gov and EUCTR posting formats
- Clinical documents like protocols, CSRs, IBs
- Safety narrative writing and PV reporting
Key Skills:
- Strong command of English language and medical/scientific terminology
- Proficiency in Microsoft Word and familiarity with document templates
- Knowledge of ICH-GCP, EMA/FDA regulations
- Good understanding of clinical trial methodology and statistical reporting
Salary & Benefits
- Salary Range: ₹4 – ₹7 LPA (Depending on skills and prior experience)
- Location: 100% Remote – Work from the comfort of your home
- Work-Life Balance: Flexible schedules and collaborative virtual environment
- Growth Opportunities: Access to global writing projects and upskilling through internal training modules
Why Medical Writing is a Great Career Option
Medical Writing has become one of the most promising career choices for pharmacy and life sciences graduates in recent years. It offers: Remote Syneos Health Hiring Clinical Trial
- Exposure to global clinical research operations
- Involvement in regulatory strategies and scientific communication
- Opportunities for working with international pharmaceutical clients
- Consistent demand across CROs, pharma companies, and medical communication firms
As regulatory frameworks become more complex, the demand for trained medical writers continues to grow, making it a stable and future-proof career option.
About Clinical Trial Disclosure & Regulatory Writing
Clinical Trial Disclosure involves making essential trial information publicly available through global registries like ClinicalTrials.gov (U.S.) or EUCTR (Europe), ensuring transparency and compliance. Remote Syneos Health Hiring Clinical Trial
Regulatory Medical Writing focuses on creating structured documentation that supports drug approvals, safety reporting, and scientific communication with health authorities like the FDA, EMA, and CDSCO.
Professionals skilled in these areas contribute directly to clinical development programs, playing a key role in bringing new therapies to market.
How to Apply
Eligible and interested candidates can apply directly through the official careers page of Syneos Health or through trusted job portals. Prepare an updated resume highlighting your regulatory writing or clinical trial disclosure experience, and include relevant keywords such as CSR writing, protocol authoring, ICH-GCP knowledge, and clinical trial transparency. Remote Syneos Health Hiring Clinical Trial
Final Thoughts
This opening at Syneos Health is an excellent opportunity for life sciences postgraduates who are looking to begin or accelerate their careers in medical writing and regulatory affairs. With remote work flexibility, exposure to global standards, and access to a supportive team, this role is well-suited for candidates who are analytical, detail-oriented, and passionate about scientific documentation. Remote Syneos Health Hiring Clinical Trial
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