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Study Data Delivery Manager

Amgen
5-8 years
Not Disclosed
Hyderabad
1 June 3, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Study Data Delivery Manager

Location: Hyderabad, India
Work Type: On-Site

Position Summary

The Study Data Delivery Manager is accountable for the management and oversight of clinical study data throughout the study lifecycle. This role leads end-to-end data management activities and ensures the delivery of high-quality, timely, and decision-ready data that supports successful clinical trial execution.

The position serves as the primary study-level data management lead, driving quality, delivery excellence, and cross-functional collaboration across global teams.


Key Responsibilities

Study Data Management Leadership

  • Serve as the single accountable lead for study-level data management activities.

  • Drive data quality, delivery timelines, and cross-functional alignment across local and global teams.

  • Lead end-to-end data management activities throughout the clinical trial lifecycle.

Data Management Planning

  • Develop and execute the Data Management Plan (DMP).

  • Lead the development and implementation of the Integrated Data Review Plan (IDRP).

  • Ensure data management strategies align with study protocols and program objectives.

Database Development & Readiness

  • Collaborate with Database Design and Data Acquisition teams on database build activities.

  • Oversee User Acceptance Testing (UAT) processes.

  • Ensure database go-live readiness and successful deployment.

Study Conduct & Data Review

  • Manage data cleaning activities throughout the study.

  • Oversee query management and issue resolution.

  • Coordinate reconciliation activities across data sources.

  • Lead database lock preparation and readiness activities.

  • Ensure studies remain delivery-ready at all stages.

Data Monitoring & Quality Oversight

  • Monitor key study data metrics, including:

    • eCRF Entry Status

    • Non-CRF Data Collection

    • Query Aging

    • Reconciliation Backlogs

    • Key Risk Indicators (KRIs)

  • Proactively identify risks and implement corrective actions.

  • Ensure timely delivery of high-quality study data.

Stakeholder Management

  • Lead study data deliverables and cross-functional data reviews.

  • Facilitate issue resolution through proactive follow-up and collaboration.

  • Communicate study data status, risks, and mitigation plans to stakeholders.


Required Qualifications

Candidates must meet one of the following educational and experience requirements:

  • Doctorate Degree, OR

  • Master’s Degree with a minimum of 2 years of experience in Life Sciences, Computer Science, or Business Administration, OR

  • Bachelor’s Degree with a minimum of 4 years of experience in Life Sciences, Computer Science, or Business Administration, OR

  • Associate Degree with a minimum of 8 years of experience in Life Sciences, Computer Science, or Business Administration, OR

  • High School Diploma/GED with a minimum of 10 years of experience in Life Sciences, Computer Science, or Business Administration.


Preferred Skills

  • Clinical Data Management experience within the pharmaceutical, biotechnology, or clinical research industry.

  • Strong understanding of clinical trial processes and data lifecycle management.

  • Experience with database build, UAT, and database lock activities.

  • Knowledge of data review, reconciliation, and query management processes.

  • Strong analytical, problem-solving, and decision-making skills.

  • Excellent stakeholder management and cross-functional collaboration abilities.

  • Strong project management and organizational skills.

  • Ability to manage multiple priorities in a fast-paced environment.

  • Excellent written and verbal communication skills.