Database Design Associate

Amgen Technology; Hyderabad; On-site; INR 600,000 - 1,200,000; Full time

Job summary

Amgen is seeking a Data Management Support professional to join our clinical research team. In this role, you will help ensure high-quality, timely, and compliant data delivery across the trial lifecycle.

You will work with EDC systems such as Veeva Vault and Medidata Rave, perform database builds, data cleaning, and query management, and collaborate with cross-functional teams to drive study outcomes. A strong background in life sciences and hands-on experience with data management in global

Qualifications

• Bachelor's degree or equivalent combination.
• Associates degree with 4 years clinical execution experience.
• High school diploma or GED with 6 years clinical execution experience.
• 2 years' life sciences experience, including 1 year in clinical research.
• Experience with data management on global clinical trials.

Responsibilities

• Support core data management activities across the study lifecycle.
• Database build, edit checks, lab and coding setup.
• Data cleaning, query management, reconciliation, and lock preparation.
• Hands-on support across build, conduct, and closeout phases.
• Monitor data quality and escalate issues, contributing to practical solutions.
• Collaborate cross-functionally and gain exposure to end-to-end data management.

Skills

Data Management

Clinical Trials

EDC Systems

Cross-functional Collaboration

Education

Bachelor's degree

Associates degree + 4 years clinical execution

High school diploma + 6 years clinical execution

Tools

Veeva Vault

Medidata Rave

Job description

Job Summary

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Responsibilities

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.

Qualifications

Basic Qualifications:

• Bachelors degree OR
• Associates degree and 4 years of clinical execution experience OR
• High school diploma / GED and 6 years of clinical execution experience

Preferred Qualifications:

• 2 years' work experience in life sciences or medically related field, including 1 years 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