Senior Manager Program Data Delivery

Amgen Inc. (IR); Hyderabad; On-site; INR 3,000,000 - 4,500,000; Full time

Job summary

Amgen Inc. (IR) is seeking a Program Data Delivery Sr Manager to provide program-level oversight for data delivery across multiple studies, ensuring database readiness, data cleaning, reconciliation, and lock execution with cross-study cohesion.

The role directs a pod of Study Data Delivery Leads and Central Monitors, driving best practices, performance consistency, and escalation when data issues arise, balancing tactical resolution with a program-wide perspective.

Qualifications

• Doctorate/Master/Bachelor/Associate/High school level + life science, computer sciences, business administration experience
• Minimum 2 years of direct people leadership experience
• Experience balancing tactical resolution with program-wide perspective

Responsibilities

• Build and maintain the program data delivery plan for all studies with milestones
• Standardize program practices for data management and reconciliation
• Lead Study Data Delivery Leads and Central Monitors
• Review program metrics and ensure actions are followed through
• Chair program-level reviews and coordinate cross-functional resolutions
• Coordinate resources and surge support to keep critical paths green
• Consolidate program risk registers and track mitigation
• Prepare program data delivery status for governance
• Mentor study-level leads in planning and stakeholder management

Skills

Leadership

Data management

Program management

Stakeholder management

Cross-functional collaboration

Mentoring

Risk management

Communication

Education

Doctorate degree

Master’s degree

Bachelor’s degree

Associate’s degree

High school diploma

Job description

Career Category Clinical Development Job Description Role Description: The Program Data Delivery Sr Manager provides program-level oversight and accountability for data delivery across multiple studies, ensuring alignment and consistency in database readiness, data cleaning, reconciliation, and lock execution. This role ensures cross-study cohesion and serves as the accountable data management voice at the program level. The Sr Manager manages and mentors a pod of Study Data Delivery Leads and Central Monitors, setting expectations, driving adoption of best practices, and ensuring performance consistency across the program to elevate quality and efficiency across the entire portfolio. This role acts as the escalation point and strategic advisor for study-level data issues, balancing tactical resolution with a program-wide perspective.

Roles & Responsibilities:

• Build and maintain the program data delivery plan covering all studies, key milestones, and inter-study dependencies.
• Standardize program practices for DMP, IDRP, query management, reconciliation, and lock procedures.
• Lead Study Data Delivery Leads and Central Monitors; provide direction, review their performance, and align their execution.
• Review program metrics (database build progress, query burden, reconciliation status, risk signals) and ensure actions have appropriate follow-through, actions, and closure.
• Chair program-level issue reviews and coordinate cross-functional resolutions with Clinical Operations, Biostats, Safety, Systems, and vendors.
• Coordinate program resources and surge support, including associates and FSPs, to keep critical paths green.
• Consolidate program risk registers and ensure mitigation plans are tracked to closure.
• Prepare program data delivery status for governance, highlighting risks, decisions, and trade-offs.
• Mentor study-level leads on planning, communication, stakeholder management, and overall execution.

Basic Qualifications and Experience:

• Doctorate Degree and 2 years of life science, computer sciences, business administration experience OR Master’s Degree and 6 years of life science, computer sciences, business administration experience OR Bachelor’s degree and 8 years of life science, computer science, business administration experience OR Associate’s degree and 10 years of life science, computer science, business administration experience OR High school diploma / GED and 12 years of life science, computer science, business administration experience
• In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.
• Your managerial experience may run concurrently with the required technical experience referenced above.

Preferred Experience:

• 7 years work experience in life sciences or medically related field, including 5 years of managing data on biopharmaceutical clinical research experience
• Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials
• Experience with managing data collection and oversight with external vendor (CROs, central labs, imaging vendors, etc.)
• Experience with risk-based monitoring models / risk-based quality management, and/or clinical site management

Functional Competencies: Must-Have Competencies:

• Demonstrates ability for end-to-end management of study deliverables, budgets, timelines, and performance metrics (KPIs) to optimize trial execution.
• Ability to identify operational risks based on protocol design and implement innovative mitigation strategies.
• Identify and manage study issues, communicating and/or escalating appropriately.
• Experience with overseeing study budgets and financial operations, reviewing/approving site expenditures, and optimizing resource allocation to ensure cost efficiencies.
• Interprets clinical and operational data to guide trial execution and identify study trends.
• Collaborates with biostatistics and data management to ensure data integrity.
• Able to identify and implement opportunities for continuous improvement into the team’s working practices.
• Experience with overseeing external vendors (Contract Research Organizations, labs, imaging vendors, etc.) to drive and meet study deliverables with high quality
• Experience with developing and training teams related to clinical trial materials (e.eg., CRAs, site staff, and cross-functional teams) to ensure alignment with study protocols, regulatory requirements, and best practices.
• Experience driving and executing change initiatives ensuring adoption of new designs within function.
• Ability to manage, mentor, and develop professionals and support staff across functions & geographies, while fostering collaboration across internal and external teams for trial success.

Soft Skills:

• Strong collaboration and communication skills to engage with cross-functional teams, senior management and external stakeholders, internally and externally.

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen