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Manager, Clinical And Safety Analytics

Bristol Myers Squibb
0-2 years
$100,000 – $140,000
Hyderabad
10 June 15, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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

Position Summary

The Analyst will support the Worldwide Patient Safety & Pharmacovigilance (PV) Center of Excellence Analytics function by developing, maintaining, and enhancing analytical reporting frameworks. The role focuses on leveraging compliance, safety, clinical, and real-world data to generate insights that improve productivity, quality, efficiency, and regulatory compliance across BMS REMS and Clinical Analytics programs.


Key Responsibilities

1. Compliance & Drug Safety Analytics

  • Ensure compliance with regulatory requirements and FDA REMS regulations.

  • Support qualitative and quantitative research projects related to drug safety and regulatory adherence.

  • Collaborate with Regulatory, Medical Safety, Clinical Safety, Commercial, and Marketing teams.

2. Data Analytics & Reporting

  • Develop, maintain, and enhance analytics solutions using:

    • Tableau

    • Spotfire

    • Excel

  • Create automated reporting solutions to reduce manual data retrieval and reporting efforts.

  • Analyze large datasets and generate actionable business insights.

3. Business Intelligence & Visualization

  • Design dashboards and visualizations for leadership and stakeholders.

  • Monitor trends, performance metrics, and operational KPIs.

  • Present findings and recommendations to management teams.

4. Real-World Data (RWD) Analytics

  • Conduct studies using clinical and real-world healthcare datasets.

  • Interpret analytical findings generated by REMS Advisory teams.

  • Develop reports and presentations for stakeholders based on study outcomes.

5. Stakeholder & Program Support

  • Understand pharmacy and prescriber operating environments.

  • Address stakeholder concerns and collaborate on process improvements.

  • Support vendor interactions, conferences, and industry engagements.

6. Audit & Compliance Support

  • Assist in audit preparation and compliance activities for REMS and Clinical programs.

  • Maintain documentation related to validation and regulatory requirements.


Required Qualifications

Education

  • Bachelor's Degree (BS/BA) required.

  • Master's Degree or advanced degree preferred.

Experience

  • 5–8 years of experience in:

    • Pharmaceutical Industry

    • Biotechnology Industry

    • Pharmacovigilance Analytics

    • Clinical Analytics

    • Healthcare Data Analytics

Domain Knowledge

  • FDA Risk Evaluation and Mitigation Strategies (REMS)

  • Drug Safety & Pharmacovigilance

  • Clinical Data Analytics

  • Real-World Data (RWD)


Technical Skills

Data Visualization

  • Tableau (Advanced)

  • Spotfire (Preferred)

  • Microsoft Excel (Advanced)

Programming

  • SQL

  • SAS

  • Python

Databases

  • Salesforce

  • PostgreSQL

  • Oracle

  • SharePoint Lists

Additional Skills

  • Data Validation

  • Dashboard Development

  • Statistical Analysis

  • Reporting Automation

  • Business Intelligence


Core Competencies

  • Strong analytical and problem-solving abilities

  • Strategic thinking and decision-making

  • Excellent presentation and communication skills

  • Project management capabilities

  • Ability to manage multiple priorities simultaneously

  • Cross-functional collaboration

  • High attention to detail

  • Strong integrity and confidentiality standards


Ideal Candidate Profile

Candidates with experience in:

  • Pharmacovigilance (PV)

  • Drug Safety Operations

  • REMS Programs

  • Clinical Data Analytics

  • Real-World Evidence (RWE)

  • Healthcare Analytics

  • Regulatory Reporting

will be highly competitive for this position.


Work Model

Depending on business requirements, the role may be:

  • Site Essential (100% onsite)

  • Site-by-Design (Hybrid)

  • Field-Based

  • Remote-by-Design


Career Growth Opportunities

Potential future career paths include:

  • Senior Analytics Manager

  • Pharmacovigilance Analytics Lead

  • Real-World Evidence (RWE) Manager

  • Clinical Data Science Manager

  • Business Intelligence Lead

  • Director, Safety Analytics


Overall Assessment

Role Level

Senior Analyst / Analytics Specialist

Difficulty Level

High

Industry

Pharmaceuticals / Biotechnology

Function

Pharmacovigilance Analytics | Clinical Analytics | Real-World Data Analytics

Recommendation

A strong opportunity for professionals with experience in Drug Safety, Pharmacovigilance, Clinical Data Analytics, Tableau, SQL, Python, and Real-World Data seeking growth within a global pharmaceutical organization.