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Senior Manager, External Data Acquisition

Bristol Myers Squibb
8-12 years
INR 30-45 LPA
Hyderabad
10 June 17, 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, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding

Position Summary

The Senior Manager, External Data Acquisition is responsible for leading the acquisition and integration of external clinical trial data from vendors, partners, and third-party sources. The role focuses on developing and implementing data collection strategies, ensuring consistency across studies, and driving process improvements that support clinical development programs.


Key Responsibilities

External Data Strategy

  • Develop and execute strategies for acquiring external clinical trial data.

  • Ensure standardized data collection processes across therapeutic areas and clinical programs.

  • Collaborate with internal and external stakeholders to optimize data acquisition workflows.

Data Management & Integration

  • Oversee collection, integration, and quality control of vendor-generated clinical trial data.

  • Ensure data standards and compliance requirements are met.

  • Support data transfer specifications and external data reconciliation activities.

Leadership & Team Development

  • Train, mentor, and support team members.

  • Provide guidance on best practices for external data acquisition.

  • Foster a culture of continuous learning and operational excellence.

Process Improvement

  • Identify opportunities for automation and smart data collection solutions.

  • Participate in continuous improvement initiatives.

  • Implement innovative approaches to improve efficiency and data quality.

Stakeholder Management

  • Partner with Clinical Data Management, Clinical Operations, Biostatistics, Programming, and external vendors.

  • Communicate project status, risks, and mitigation strategies effectively.

  • Ensure alignment between business objectives and data acquisition activities.


Required Qualifications

Education

  • Bachelor's Degree required.

  • Degree in Life Sciences, Data Integration, Computer Science, Health Sciences, or related scientific discipline preferred.

Experience

  • Significant experience in Clinical Data Management, External Data Acquisition, or Clinical Research.

  • Experience managing vendor-generated clinical trial data.

  • Strong understanding of clinical development processes and industry standards.

  • Experience leading projects and mentoring teams.

Technical Skills

  • Knowledge of clinical trial data standards and integration processes.

  • Understanding of external data sources such as:

    • Central Labs

    • Imaging Vendors

    • ePRO/eCOA Systems

    • Wearables and Digital Health Technologies

    • Biomarker Data Providers

  • Familiarity with clinical databases and data management systems.

Soft Skills

  • Strong leadership and people management skills.

  • Excellent communication and stakeholder management abilities.

  • Strategic thinking and problem-solving capabilities.

  • Ability to work in a cross-functional global environment.


Preferred Qualifications

  • Experience in pharmaceutical, biotechnology, or CRO environments.

  • Knowledge of regulatory requirements and GxP guidelines.

  • Experience driving process transformation and innovation initiatives.


Work Arrangement

Occupancy Model

  • Site-Essential: 100% onsite.

  • Site-by-Design: Hybrid model with at least 50% onsite presence.

  • Field-Based/Remote-by-Design: Travel may be required for business meetings and stakeholder interactions.


Why Join Bristol Myers Squibb?

  • Work on life-changing therapies and clinical innovations.

  • Global career growth opportunities.

  • Collaborative and inclusive work culture.

  • Competitive compensation and benefits.

  • Exposure to cutting-edge clinical technologies and data strategies.

BMS Mission

"Transforming Patients' Lives Through Science™"