PHARMAFull-time
Medical Writer I / Medical Writer II (CSR Narratives)
By Admin · Medical & Scientific Writing
DELHI NCR (IN)REMOTEPOSTED: 9/25/2026
PHARMAFull-time
HIRING ORGANIZATIONSYNEOS HEALTHBiopharmaceutical / Healthcare Services
ROLE OVERVIEW
Medical writing role focused on drafting and reviewing clinical and patient narratives and other clinical-development documents. The position supports high-quality regulatory documentation and collaboration across data management, biostatistics, regulatory affairs and medical affairs.
ROLE DEFINITION & RESPONSIBILITIES
- •Compile, write and edit medical writing deliverables with minimal supervision
- •Draft and review patient and clinical narratives
- •Develop or support clinical study protocols, protocol amendments, clinical study reports, annual reports and investigator brochures
- •Review statistical analysis plans and table, figure and listing specifications for content, grammar, format and consistency
- •Collaborate with data management, biostatistics, regulatory affairs and medical affairs teams
- •Conduct peer reviews and address review comments for scientific accuracy, clarity and consistency
- •Perform clinical literature searches and apply relevant regulatory guidance and company/client standards
- •Mentor less experienced medical writers where required
Reporting Hierarchy: Works within Syneos Health Clinical Solutions and collaborates with data management, biostatistics, regulatory affairs, medical affairs and medical-writing leadership; specific line manager not stated
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Minimum 1 year of narrative-writing experience with a master's qualification or 2 years with a bachelor's degree
- Master's/MPharm or bachelor's degree
- Strong experience drafting and reviewing narratives
- Strong knowledge of English grammar
- Knowledge of FDA and ICH regulations and guidelines
- Familiarity with AMA style guide
- Ability to interpret and present clinical data and complex information
- Strong proficiency in Word, Excel, PowerPoint, email and Internet
PREFERRED QUALIFICATIONS
- •Clinical research principles
- •Experience with clinical study reports and related documents
- •Knowledge of ICH-E3
- •Experience with regulatory medical writing
- •Literature-search experience
- •Demonstrated presentation, proofreading and leadership skills
REQUIRED VERIFIED SKILLS
Medical writing
CSR narratives
patient narratives
clinical study reports
clinical protocols
ICH-E3
FDA regulations
ICH guidelines
AMA style
clinical research
clinical data interpretation
proofreading
literature searching
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Career development and progression; supportive line management; technical and therapeutic-area training; peer recognition; total rewards; inclusive work environment
No salary range is disclosed in the supplied posting. Compensation should therefore be treated as undisclosed rather than estimated.
ORGANIZATION CONTEXT & CULTURE
Syneos Health is a global life sciences services organization providing integrated clinical development and commercialization services to pharmaceutical and healthcare organizations.
TEAM SIZE: 25,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare Services
Culture: Syneos Health describes an agile, collaborative and inclusive environment focused on customer success, innovation, professional development and improving patient progress.
EXPECTED CAREER ROADMAP
Potential progression may include Medical Writer II, Senior Medical Writer and broader medical-writing or regulatory-document leadership roles, depending on experience, performance and organizational opportunities.
APPLICATION ADVISORY
Emphasize hands-on narrative drafting and review experience, clearly distinguish master's versus bachelor's experience requirements, highlight ICH/FDA knowledge, clinical data interpretation, proofreading and document-review skills, and demonstrate familiarity with CSR and patient-narrative standards.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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