Opportunity for B. Pharma/ M. Pharma/ Pharma D/ Ph D/ B. Sc/ M. Sc as a Scientific Writer II at Bristol Myers Squibb – Apply Now

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Unlock your potential with Bristol Myers Squibb! We’re on the lookout for talented individuals in the pharmaceutical field – whether you hold a B.Pharm, M.Pharm, Pharma D, or Ph.D. Bristol Myers Squibb is hiring for the role of Scientific Writer II. If you’re passionate about communicating scientific insights and making a difference in healthcare, join our team and be part of pioneering advancements in the industry. Discover how you can contribute to groundbreaking research and innovation at Bristol Myers Squibb as a Scientific Writer II.

Position Summary

To coordinate and author documents needed for regulatory submissions, ensuring the coordination and integration of the scientific, medical, and regulatory input from cross-functional team members.

Key Responsibilities

• Coordinate and author regulatory documents [eg, Investigator’s Brochures (IB), development safety update reports, periodic benefit-risk evaluation reports, clinical study reports (CSR), protocols, and high-level summary documents] ensuring the coordination and integration of the scientific, medical, and regulatory input from development team members.
• Participate in relevant document subteam(s) and ensure effective planning and management of timelines for all components of assigned documents.
  Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects.
• Maintain document prototypes and shells.
• Comply with internal and external processes and guidelines while managing the review process and, on an ongoing basis, resolve issues, errors, or inconsistencies with pertinent team members to ensure timely completion and high quality of assigned documents.
• Review and edit documents as required.

Skill & Knowledge

• Demonstrated strong writing skills in authoring and managing the production of IB, Safety Aggregate Report, Clinical Protocols, and/or CSR.
• Ability to analyze and interpret complex data from a broad range of scientific disciplines.
• Understanding of global pharmaceutical drug development.
• Demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation, and interpersonal skills in a cross-functional team.
• Working knowledge of a document management system and basic knowledge of the document publishing process.

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