Data Delivery Lead

Amgen; Hyderabad; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Amgen in Hyderabad is seeking a data management leader for clinical trials. You will be accountable for overseeing data management processes and ensuring timely, high-quality data delivery.

The candidate should have relevant educational qualifications and experience in life sciences or clinical research, with a strong focus on cross-functional alignment and quality assurance.

Qualifications

• Doctorate Degree OR Master's with 2 years relevant experience.
• Bachelor's with 4 years, Associate's with 8 years, or High school with 10 years in life sciences.
• 5 years' experience preferred in life sciences or clinical research.

Responsibilities

• Manage end-to-end data management for clinical trials.
• Oversee study conduct activities including data cleaning and query management.
• Drive development and execution of data management plans.

Skills

Data management

Clinical research

Cross-functional leadership

Quality assurance

Education

Doctorate, Master's, Bachelor's, Associate's degree, or High school diploma with relevant experience

Job description

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

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.)