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Manager, Clinical And Safety Analytics

Bristol Myers Squibb
Bristol Myers Squibb
5-8 years
Not Disclosed
Hyderabad
10 March 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description

Position Summary
The Manager, Clinical and Safety Analytics is responsible for developing and enhancing analytical frameworks to support reporting and insights within the Worldwide Patient Safety and Pharmacovigilance analytics function. The role focuses on analyzing compliance and safety data to generate insights related to productivity, efficiency, and quality that support informed decision-making across clinical safety programs.

This position supports analytics initiatives related to Risk Evaluation and Mitigation Strategies (REMS), clinical data reporting, and real-world data analysis while collaborating with cross-functional teams across regulatory, medical, and commercial functions.

Key Responsibilities

Develop and enhance analytics frameworks to support clinical safety and pharmacovigilance reporting

Ensure compliance with regulatory requirements related to drug safety and REMS programs

Maintain and develop reporting and analytics applications using tools such as Tableau, Spotfire, and Excel

Leverage internal data systems and analytics tools to automate data visualization and reporting processes

Aggregate and analyze clinical and safety data to generate actionable insights and answer key business questions

Develop and maintain reports on activities, outcomes, and safety trends for leadership and stakeholders

Prepare and deliver presentations based on analytical findings to management and cross-functional teams

Analyze stakeholder feedback and complaints and collaborate with relevant teams to propose solutions

Interpret analytical findings and contextualize insights generated by internal REMS advisory teams

Conduct real-world data analysis studies and present outcomes to internal stakeholders

Support audit activities related to clinical safety, pharmacovigilance, and REMS programs

Professional Experience Requirements

5–8 years of experience in pharmaceutical, biotechnology, clinical research, or pharmacovigilance analytics roles

Understanding of FDA Risk Evaluation and Mitigation Strategies (REMS) regulations and safety reporting frameworks

Experience working with analytics tools such as Tableau, Spotfire, Excel, and database systems

Knowledge of programming languages such as SAS, SQL, or Python

Experience working with clinical data and real-world healthcare data analytics

Strong analytical thinking, data interpretation, and reporting skills

Ability to work on multiple projects and collaborate with cross-functional stakeholders

Apply Details

Apply via the company career portal for
Bristol Myers Squibb