Study Data Deliver Mgr

Amgen; Hyderabad; On-site; INR 7,662,835 - 10,536,398; Full time

Benefits offered by this job

Comprehensive employee benefits package

Discretionary annual bonus program

Stock-based long-term incentives

Award-winning time-off plans

Flexible work models

Job summary

Amgen is seeking a Data Delivery Lead in Hyderabad, India, to manage and oversee data collection in clinical trials. You will drive the quality and delivery of data as a single accountable leader, ensuring that timely and reliable data supports successful trial delivery.

The ideal candidate will have a doctorate or relevant experience in life sciences, with a strong focus on cross-functional collaboration and problem-solving. Amgen provides a competitive benefits package and supportive work environment.

Qualifications

• 5 years’ work experience in life sciences or medically related field.
• 3 years of biopharmaceutical clinical research experience on clinical trials.
• Experience managing external vendors.

Responsibilities

• Lead management and oversight of study-level data.
• Drive quality and delivery in data management processes.
• Monitor study data metrics and resolve issues.

Skills

Leadership in data management

Data cleaning and quality assurance

Cross-functional collaboration

Problem-solving skills

Education

Doctorate Degree

Master’s Degree with 2 years of experience

Bachelor’s degree with 4 years of experience

Associate’s degree with 8 years of experience

High school diploma / GED with 10 years of experience

Job description

Data Delivery Lead

Let’s do this. Let’s change the world. In this vital role you are accountable for the management and oversight of data collected within a study/program. You will lead end‑to‑end data management and ensure high‑quality, timely, and decision‑ready data that enables successful clinical trial delivery.

• Serve as the single accountable leader for study‑level data management, driving quality, delivery, and cross‑functional alignment, locally and globally.
• Lead development and execution of the Data Management Plan and Integrated Data Review Plan (IDRP) aligned to protocol and program strategy.
• Drive database build, UAT, and go‑live readiness in partnership with Database Design and Acquisition teams.
• Oversee study conduct activities including data cleaning, query management, reconciliation, and database lock preparation, ensuring we are “delivery ready” at all times.
• Monitor study data metrics (e.g., eCRF entry, Non‑CRF data collection, query aging, reconciliation backlog, KRIs) and proactively resolve issues to ensure on‑time delivery.
• Lead data deliverables, proactive in follow up, ensuring issue resolution and high‑quality outputs.

What We Expect Of You

The candidate we seek is an individual with the following qualifications.

Basic Qualifications

• Doctorate Degree OR
• Master’s Degree and 2 years of life science, computer sciences, business administration experience OR
• Bachelor’s degree and 4 years of life science, computer science, business administration experience OR
• Associate’s degree and 8 years of life science, computer science, business administration experience OR
• High school diploma / GED and 10 years of life science, computer science, business administration experience

Preferred Qualifications

• 5 years’ work experience in life sciences or medically related field, including 3 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company.
• Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials.
• Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.).

What You Can Expect Of Us

From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

• Comprehensive employee benefits package, including a retirement and savings plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales‑based incentive plan.
• Stock‑based long‑term incentives.
• Award‑winning time‑off plans and bi‑annual company‑wide shutdowns.
• Flexible work models, including remote work arrangements, where possible.

Amgen is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.