Data Management Associate

Amgen Inc; Hyderabad; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Amgen Inc in Hyderabad is seeking a Data Management Support professional to execute core data management activities across the clinical trial lifecycle, ensuring timely, high-quality data delivery for study outcomes.

The role includes database build, edit checks, data cleaning, query management, reconciliation, and lock readiness, with exposure to Veeva Vault and Medidata Rave and cross-functional collaboration.

Qualifications

• Bachelor's degree with 4 years of clinical execution experience.
• Experience in data management on global clinical trials.
• 2 years' work experience in life sciences or medially related field, including 1 year of biopharmaceutical clinical research experience.

Responsibilities

• Support execution of core data management activities across the study lifecycle, including database build, edit check testing, lab and coding setup, data cleaning, query management, reconciliation, and lock preparation.
• Provide hands‑on, flexible support across build, conduct, and closeout phases, developing broad exposure to end‑to‑end data management processes and study delivery.
• Deliver accurate and timely completion of assigned tasks, eg query management in support of Data Delivery.
• Assist in the preparation and maintenance of study documentation, including CRF testing scripts, reconciliation trackers and lock readiness materials.
• Monitor data quality and query trends, proactively identifying issues, escalating where appropriate, and contributing to practical solutions.
• Collaborate cross‑functionally when required, building proficiency in EDC systems (e.g. Veeva Vault, Medidata Rave) and other data management tools.

Skills

Data management

Collaboration

Education

Bachelor's degree

Tools

Veeva Vault

Medidata Rave

Job description

Data Management Support

What you will do

Lets do this. Lets change the world. In this vital role you will support the execution of core data management activities across the clinical trial lifecycle, ensuring high-quality, timely, and compliant data delivery to enable effective study outcomes and decision-making.

• Support execution of core data management activities across the study lifecycle, including database build, edit check testing, lab and coding setup, data cleaning, query management, reconciliation, and lock preparation.
• Provide hands‑on, flexible support across build, conduct, and closeout phases, developing broad exposure to end‑to‑end data management processes and study delivery.
• Deliver accurate and timely completion of assigned tasks, eg query management in support of Data Delivery.
• Assist in the preparation and maintenance of study documentation, including CRF testing scripts, reconciliation trackers and lock readiness materials.
• Monitor data quality and query trends, proactively identifying issues, escalating where appropriate, and contributing to practical solutions.
• Collaborate cross‑functionally when required, building proficiency in EDC systems (e.g. Veeva Vault, Medidata Rave) and other data management tools.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.

Basic Qualifications

• Bachelors degree with 4 years of clinical execution experience

Preferred Qualifications

• 2 years' work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
• Experience working in Data Management on global clinical trials