PHARMAFull-time
Scientific Writer II
By Admin · Medical & Scientific Writing
HYDERABAD (IN)ONSITEPOSTED: 9/24/2026
PHARMAFull-time
HIRING ORGANIZATIONBRISTOL MYERS SQUIBBPharmaceuticals
BR
ROLE OVERVIEW
Author and coordinate high-quality regulatory and clinical documents by integrating scientific, medical, and regulatory input across cross-functional development teams. The role combines scientific writing, document strategy, timeline management, quality review, and regulatory documentation expertise.
ROLE DEFINITION & RESPONSIBILITIES
- •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 and regulatory writing skills
- •Demonstrated experience authoring or managing Investigator's Brochures, Safety Aggregate Reports, Clinical Protocols, and/or Clinical Study Reports
- •Ability to analyze and interpret complex scientific data
- •Understanding of global pharmaceutical drug development
- •Strong organizational, communication, facilitation, and interpersonal skills
- •Ability to manage timelines and quality in cross-functional teams
- •Working knowledge of document management systems and basic document publishing processes
Reporting Hierarchy: Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for serious diseases. The company emphasizes patient impact, scientific innovation, collaboration, inclusion, wellbeing, and professional growth.
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- PhD in biological sciences or PharmD
- Experience across multiple regulatory document types
- Experience with document publishing workflows
- Familiarity with global regulatory requirements
- Experience working in cross-functional pharmaceutical development teams
PREFERRED QUALIFICATIONS
- •Reports within the Scientific/Medical Writing organization and works cross-functionally with clinical, medical, regulatory, safety, and development team members
- •Coordinates document activities across assigned project teams
REQUIRED VERIFIED SKILLS
PharmD
PhD biological sciences
regulatory submissions
cross-functional facilitation
document lifecycle management
timeline management
editing
scientific communication
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Supportive work environment; comprehensive benefits; wellbeing support; flexible working options; career growth and development opportunities; inclusive workplace culture
Highlight regulatory and scientific writing experience; list specific documents authored or managed such as IBs, DSURs, PBRERs, protocols, and CSRs; demonstrate ability to interpret complex scientific data; emphasize global drug-development knowledge; showcase timeline management and cross-functional collaboration; mention document management and publishing-system experience; include PharmD/PhD credentials prominently where applicable.
ORGANIZATION CONTEXT & CULTURE
Biopharmaceuticals
TEAM SIZE: BMS describes a purpose-driven culture centered on collaboration, accountability, urgency, inclusion, wellbeing, flexibility, innovation, and meaningful patient impact.
INDUSTRY: Pharmaceuticals
Culture: Rolling admissions
EXPECTED CAREER ROADMAP
The supplied job posting does not disclose a salary range, bonus, or equity information, so no compensation figures are provided.
APPLICATION ADVISORY
[https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Scientific-Writer-II_R1606692/apply?locationHierarchy2=7b0045a3289810548a41236822339065
RECOMMENDED TRAINING
1/2
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