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Clinical Data Manager

Bristol Myers Squibb
2+ years
INR 8 LPA – 14 LPA
Hyderabad
1 July 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Clinical Data Manager

Company: Bristol Myers Squibb (BMS)
Location: Hyderabad, Telangana, India
Department: Clinical Data Management
Job Type: Full-Time (Hybrid)


JOB OVERVIEW

The Clinical Data Manager is responsible for ensuring the accuracy, completeness, consistency, and integrity of clinical trial data throughout the study lifecycle. The role involves clinical data review, query management, external data reconciliation, data cleaning, CRF management, eTMF documentation, and coordination with cross-functional teams and external vendors to support timely database lock and high-quality clinical trial deliverables in compliance with GCP and regulatory standards.


KEY RESPONSIBILITIES

Clinical Data Review

  • Review clinical study protocols and data review plans.

  • Analyze clinical data listings for quality and completeness.

  • Perform ongoing clinical data review and validation.

  • Identify and resolve data discrepancies.

  • Ensure data accuracy and consistency throughout the study.

Data Cleaning

  • Perform data cleaning activities according to study requirements.

  • Manage discrepancy resolution and query processing.

  • Execute Clean Patient Group (CPG) activities.

  • Verify data completeness before database lock.

  • Ensure high-quality clinical datasets.

Query Management

  • Generate, review, and resolve data queries.

  • Coordinate query resolution with study teams.

  • Track outstanding queries until closure.

  • Maintain query turnaround timelines.

  • Support efficient data review processes.

CRF Management

  • Review Case Report Forms (CRFs).

  • Freeze and lock CRFs and data fields.

  • Ensure timely completion of CRF activities.

  • Verify data captured in electronic CRFs (eCRFs).

  • Maintain data quality throughout the study lifecycle.

External Data Management

  • Review external vendor data uploads.

  • Monitor external data transfer schedules.

  • Reconcile external clinical data.

  • Coordinate discrepancy resolution with external vendors.

  • Ensure integration of external datasets into study databases.

Documentation Management

  • Maintain Trial Master File (eTMF) documentation.

  • File study documents according to the eTMF Master Plan.

  • Maintain accurate clinical documentation.

  • Ensure inspection-ready documentation.

  • Support audit and regulatory compliance.

Study Coordination

  • Coordinate with Clinical Data Management Leads.

  • Support study milestones and deliverables.

  • Participate in database lock activities.

  • Assist with study startup and closeout activities.

  • Monitor progress of assigned studies.

Cross-Functional Collaboration

  • Collaborate with Clinical Operations.

  • Work with Biostatistics teams.

  • Coordinate with Medical Monitors.

  • Interact with Data Management Leads.

  • Communicate with external data vendors.

  • Support cross-functional project activities.

Compliance & Quality

  • Ensure compliance with ICH-GCP guidelines.

  • Follow SOPs and Data Quality Management Plans.

  • Maintain data integrity throughout the clinical trial.

  • Support inspection and audit readiness.

  • Adhere to regulatory and company quality standards.


EDUCATIONAL QUALIFICATIONS

Required

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Biochemistry

    • Biomedical Sciences

    • Nursing

    • Related Healthcare or Scientific Discipline

Preferred

  • Master's Degree in Life Sciences or related discipline.


EXPERIENCE REQUIREMENTS

Required

  • Experience in Clinical Data Management.

  • Experience reviewing clinical trial data.

  • Experience with query management and data cleaning.

  • Knowledge of electronic data capture (EDC) systems.

  • Experience working with external clinical data.

Preferred

  • Experience with eTMF systems.

  • Experience supporting database lock activities.

  • Experience in global clinical trials.

  • Experience working with CROs or pharmaceutical companies.