Data Delivery Lead

Amgen Inc; Hyderabad; On-site; INR 1,200,000 - 2,000,000; Full time

Job summary

Amgen Inc is looking for a Data Management leader in Hyderabad, India. You will be responsible for managing data quality and ensuring prompt delivery in clinical trials.

The ideal candidate will have experience in clinical research within biopharmaceuticals and a relevant degree. Strong leadership in cross-functional team dynamics is essential. Your role will include overseeing data deliverables and resolving issues proactively to meet timelines.

Qualifications

• Doctorate degree or relevant experience in life sciences or related field.
• Minimum of 2 years experience in data management in life sciences.
• Strong leadership skills in managing clinical trials.

Responsibilities

• Manage and oversee data management within clinical trials.
• Ensure timely and quality data delivery for successful trials.
• Lead the development of the Data Management and Integrated Data Review Plans.

Skills

Clinical trial management

Data management

Cross-functional leadership

Education

Doctorate Degree

Master's Degree with 2 years experience

Bachelor's Degree with 4 years experience

Job description

Overview

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.

Responsibilities

• 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

Basic Qualifications

• Doctorate Degree OR
• Masters Degree and 2 years of life science, computer sciences, business administration experience OR
• Bachelors degree and 4 years of life science, computer science, business administration experience OR
• Associates 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.)