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Manager Program Data Support

Amgen
Amgen
5+ years
₹25 LPA – ₹40 LPA
Hyderabad
10 March 16, 2026
Job Description
Job Type: Full Time Education: PharmD/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

Manager – Program Data Support

Company: Amgen
Location: Hyderabad, Telangana, India
Job Type: Full-Time | On-Site
Experience: 5+ Years (Clinical Data Management / Clinical Data Operations)
Qualification: Bachelor’s / Master’s / Doctorate Degree in Life Sciences, Clinical Data Management, or related field
Approx Salary: ₹25 LPA – ₹40 LPA


Job Overview

Amgen is seeking a Manager – Program Data Support to lead a team responsible for supporting clinical data management operations across multiple studies and programs.

The role focuses on team leadership, resource allocation, stakeholder collaboration, and ensuring high-quality clinical data management activities throughout the clinical trial lifecycle. The manager will ensure efficient execution of startup and operational data management tasks while maintaining compliance with regulatory and quality standards.


Key Responsibilities

1. Team Management & Leadership

  • Recruit, onboard, and train Data Management Associates and Senior Associates.

  • Provide coaching, mentoring, and career development for team members.

  • Manage risks related to attrition, performance challenges, and skill gaps.

  • Foster a culture of collaboration, accountability, and continuous improvement.

2. Resource Allocation & Program Support

  • Work with resourcing leads to allocate team members based on skills, workload, and study requirements.

  • Monitor team capacity and forecast future resource demand.

  • Ensure associates are properly trained and prepared for study assignments.

  • Track allocation efficiency and adjust staffing plans when needed.

3. Clinical Data Management Operations

  • Oversee clinical data management activities across multiple clinical studies.

  • Ensure execution of startup activities, data review, cleaning, and reconciliation processes.

  • Maintain high-quality standards for clinical trial data accuracy and completeness.

4. Stakeholder Collaboration

  • Act as a point of contact for escalations related to team performance or quality issues.

  • Collaborate with study teams, program stakeholders, and resourcing partners.

  • Maintain clear communication on priorities, timelines, and deliverables.

5. Capability Development & Process Improvement

  • Identify gaps in skills, processes, or tools and drive targeted training initiatives.

  • Implement standard operating procedures, templates, and playbooks for consistent execution.

  • Capture lessons learned to improve efficiency and reduce operational errors.

6. Quality & Compliance

  • Ensure adherence to SOPs, work instructions, and quality standards.

  • Support audit and inspection readiness by maintaining traceable documentation.

  • Monitor quality metrics such as cycle time, error rates, rework, and backlog levels.


Required Skills

Technical & Functional Skills

  • Strong understanding of clinical trial execution and clinical data management processes

  • Experience with clinical data platforms and data management workflows

  • Proficiency in Microsoft Excel and data analysis tools

  • Familiarity with datasets, edit checks, discrepancy management, and reconciliation processes

Leadership & Operational Skills

  • Team management and performance development

  • Resource planning and operational prioritization

  • Stakeholder communication and conflict resolution

  • Structured problem-solving and process optimization


Preferred Experience

  • Experience supporting multiple clinical studies or programs simultaneously

  • Background in clinical data management for interventional trials

  • Experience with external data acquisition and database build processes

  • Experience managing global or remote teams across multiple time zones


Key Competencies

  • Clinical data management and data operations

  • Resource planning and team leadership

  • Quality assurance and regulatory compliance

  • Operational execution and prioritization

  • Cross-functional collaboration in global pharmaceutical programs


About the Company

Amgen is a global biotechnology leader focused on developing innovative medicines for serious illnesses. With more than 40 years of scientific innovation, the company continues to advance healthcare through biotechnology research, genetic science, and data-driven drug development.