Data Management Sr Associate

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

Job summary

Amgen Inc in Hyderabad seeks a Sr Data Management Support professional to ensure the high-quality delivery of clinical trial data. You will execute core data management tasks, support key roles, and coordinate with global teams to maintain timelines and data integrity.

The ideal candidate has a Bachelor's degree and at least 6 years of clinical execution experience, preferably with a background in life sciences or biopharmaceutical research. Join us in making a difference!

Qualifications

• 6 years of clinical execution experience.
• Experience in life sciences or medically related field.

Responsibilities

• Execute study data management tasks including database build testing and data cleaning.
• Support core Data Management roles with high-quality execution.
• Contribute to setup and maintenance of EDC/non CRF data structures.
• Track progress against data management timelines and identify risks.
• Coordinate with internal and global teams and external partners.
• Identify opportunities to improve processes and share knowledge.

Skills

Data management

Query management

Data cleaning

Clinical execution

Education

Bachelor's degree

Job description

Sr Data Management Support

Lets do this. Lets change the world. In this vital role you will support the delivery of high-quality clinical trial data by executing core data management activities across the study lifecycle, ensuring data integrity, compliance, and timely study execution.

What you will do

• Execute study data management tasks including database build testing, data cleaning, query management, reconciliation, and lock preparation with limited oversight
• Support core Data Management roles, such as Data Delivery Leads, Database Designers, and Data Acquisition Leads by owning time-sensitive deliverables with high-quality execution
• Actively contribute to setup and maintenance of EDC/non CRF data structures including local labs, coding dictionaries, along with non-CRF data integrations
• Track progress against data management timelines, study timelines and deliverables, identify risks or delays, and escalation issues with clear documentation and any mitigations
• Coordinate with local internal teams, global team members as well as external partners (including FSPs) when required to ensure aligned and efficient delivery of all study activities
• Identify opportunities to improve repeatable processes and contribute to best practices and knowledge sharing across the team

Basic Qualifications

• Bachelors degree with 6 years of clinical execution experience

Preferred Qualifications

• 3 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