Senior Medical Writer Vacancy | Syneos Health | Medical Information Writing
Syneos Health Hiring Senior Medical Writer in Gurgaon | Medical Writing Jobs
Syneos Health has announced recruitment for the position of Senior Medical Writer in Gurgaon, Haryana. This opportunity is ideal for experienced professionals from life sciences, pharmacy, biotechnology, medical communications, and clinical research backgrounds who are looking to build careers in regulatory medical writing, scientific communication, clinical documentation, and pharmaceutical publishing.
Candidates with 3–5 years of experience in medical writing, regulatory documentation, clinical study reporting, scientific publications, and healthcare communications are encouraged to apply for this hybrid full-time opportunity.
This role offers excellent exposure to global clinical development programs, regulatory submissions, scientific publications, healthcare analytics, pharmaceutical operations, medical affairs, and healthcare communication systems.
About Syneos Health
Syneos Health is a globally recognized life sciences services organization specializing in clinical development, healthcare consulting, medical communications, regulatory affairs, and pharmaceutical commercialization.
The company supports pharmaceutical companies, biotechnology organizations, medical device firms, and healthcare institutions through advanced clinical solutions, healthcare analytics, scientific communication, and regulatory support services.
Syneos Health is known for its expertise in clinical research, regulatory writing, medical affairs, scientific publishing, healthcare strategy, and patient-focused healthcare innovation.
Working at Syneos Health provides professionals exposure to international clinical trials, global healthcare systems, medical writing projects, pharmaceutical compliance operations, and healthcare technology platforms.
Senior Medical Writer Vacancy Details
Position
Senior Medical Writer
Employment Type
Full-Time
Work Model
Hybrid
Location
Gurgaon
Experience Required
3–5 Years
Job Role and Responsibilities
Selected candidates will support scientific writing, regulatory documentation, medical communications, and healthcare publication activities.
Key Responsibilities
- Mentors and leads less experienced medical writers on complex projects, as necessary.
- Acts as lead for assigned med info writing projects.
- Manages and coordinates medical information activities within and across departments with minimal supervision
- Responds to escalated queries from client internal and external teams (HCPs, patients, caregivers)
- Create or update an existent global standard scientific response communications (gSSRCs)/FAQs/global response documents/global guidance documents/local response documents based on client provided template or as per style guide
- Conducts literature search on PubMed, and/or other client-subscribed databases; and validate relevant inclusions
- Experience in developing or supporting a variety of documents that include, but not limited to:
- Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations.
- Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
- Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
- Serves as peer reviewer on internal review team providing review comments on draft and final documents.
- Adheres to established regulatory standards, including but not limited to Journal/congress specific guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
- Familiarity with figure-creation and data visualization software, including tools such as GraphPad Prism and Adobe Illustrator, for developing high-quality scientific figures and graphics.
- Familiarity with publication planning software e.g. Datavision and PubConnect (VeevaVault Promomats)
- Reviews deliverables for scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets.
- Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.
- Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
- Completes required administrated tasks within the specified timeframes.
- Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).
Eligibility and Qualifications
Candidates applying for this Senior Medical Writer role should possess strong scientific writing and regulatory documentation expertise.
Required Qualification
B.Pharm, M.Pharm, PharmD, MSc Life Sciences, MSc Biotechnology, MSc Clinical Research, MSc Pharmacology, PhD Life Sciences, MD, MBBS
Experience Required
3–5 years of relevant experience in medical writing, scientific writing, or regulatory documentation.
Required Skills
- Strong knowledge of FDA and ICH guidelines
- Experience in regulatory and scientific writing
- Expertise in clinical study documentation and reporting
- Excellent English grammar and communication skills
- Knowledge of AMA Manual of Style
- Ability to manage multiple medical writing projects
- Experience working with cross-functional healthcare teams
- Scientific literature review and data interpretation skills
- Attention to detail and healthcare compliance awareness
Preferred Experience
- Experience in biopharmaceutical, CRO, or medical device companies
- Exposure to regulatory submissions and scientific publishing
- Knowledge of medical affairs and publication planning
- Experience mentoring junior medical writers
Professionals with expertise in clinical documentation, regulatory affairs, healthcare analytics, scientific communications, and pharmaceutical operations are encouraged to apply.
Location and Salary
Location
Gurgaon
Salary
The estimated salary for Senior Medical Writer roles generally ranges between ₹10 LPA and ₹22 LPA depending on therapeutic expertise, regulatory writing experience, and clinical documentation exposure.
How to Apply
Interested candidates can apply through the official Syneos Health careers portal using the application link below:
Candidates should ensure all educational details, therapeutic expertise, and medical writing experience are updated before submitting the application.
Frequently Asked Questions
What experience is required for this Syneos Health role?
Candidates must have 3–5 years of experience in medical writing or scientific documentation.
What qualifications are preferred?
Candidates with pharmacy, biotechnology, life sciences, medical, or clinical research backgrounds can apply.
What is the work model for this role?
The role follows a hybrid work model.
What is the salary range for this role?
The estimated salary range is ₹10 LPA to ₹22 LPA depending on experience and therapeutic expertise.
What departments can candidates grow into after this role?
Candidates can build careers in Regulatory Affairs, Medical Affairs, Scientific Communications, Publication Planning, and Clinical Research Operations.
Syneos Health Senior Medical Writer Recruitment Overview
| Company | Syneos Health |
|---|---|
| Department Vacancies | Senior Medical Writer |
| Qualification | B.Pharm, M.Pharm, PharmD, MSc Life Sciences, MBBS |
| Experience | 3–5 Years |
| Location | Gurgaon |
To apply for this job please visit syneoshealth-clinicalcareers.ttcportals.com.
