PHARMAFull-time
Scientific Writer II
HYDERABAD (IN)ONSITEPOSTED: 9/29/2026
PHARMAFull-time
HIRING ORGANIZATIONBRISTOL MYERS SQUIBBPharmaceuticals
BR
ROLE OVERVIEW
Scientific Writer II responsible for authoring and coordinating regulatory and clinical documents, integrating scientific, medical, and regulatory input while managing document strategy, review cycles, timelines, quality, and compliance.
ROLE DEFINITION & RESPONSIBILITIES
- •Coordinate and author regulatory and clinical documents including IBs, safety reports, CSR documents, and protocols
- •integrate scientific, medical, and regulatory input from development teams
- •participate in document subteams and manage document timelines
- •contribute to document strategy, messaging, flow, logic, and consistency
- •maintain document prototypes and shells
- •coordinate review processes and resolve document issues, errors, and inconsistencies
- •review and edit documents to ensure quality and compliance
Reporting Hierarchy: Works within cross-functional development teams and document subteams, coordinating scientific, medical, regulatory, and other stakeholder inputs for assigned documents
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- PharmD or PhD in a relevant scientific discipline, or Bachelor's/Master's degree with approximately 2-4 years of regulatory documentation experience
- strong scientific writing experience involving IBs, safety aggregate reports, clinical protocols, and/or CSRs
- ability to analyze and interpret complex scientific data
- understanding of global pharmaceutical drug development
- strong organizational, communication, facilitation, and interpersonal skills
- working knowledge of document management systems and basic document publishing processes
PREFERRED QUALIFICATIONS
- •Experience with multiple regulatory document types
- •broader knowledge of global regulatory requirements
- •experience coordinating cross-functional document teams
- •familiarity with document publishing workflows and regulatory submission processes
REQUIRED VERIFIED SKILLS
Regulatory writing
scientific writing
medical writing
regulatory documentation
Investigator's Brochure
DSUR
PBRER
clinical study reports
clinical protocols
document management
document publishing
data interpretation
pharmaceutical drug development
project coordination
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Comprehensive benefits; wellbeing support; flexible work environment; professional growth opportunities; inclusive and collaborative culture
No compensation figures were disclosed in the provided job posting.
ORGANIZATION CONTEXT & CULTURE
Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for serious diseases.
TEAM SIZE: 30,000+
INDUSTRY: Pharmaceuticals
Culture: Purpose-driven, collaborative, inclusive, patient-focused environment emphasizing accountability, innovation, wellbeing, flexibility, and professional development.
EXPECTED CAREER ROADMAP
Opportunity to progress in medical and regulatory writing through increasing ownership of complex regulatory documents, document strategy, cross-functional leadership, and global drug development programs.
APPLICATION ADVISORY
Emphasize regulatory writing experience, strong scientific writing samples, experience with IBs/CSRs/protocols/safety reports, knowledge of global drug development, document management systems, and cross-functional coordination.
RECOMMENDED TRAINING
1/3
READY TO SUBMIT?
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