Data Management Sr Associate
Posted Updated
Job Summary
Role
What you will do
What we expect of you
Basic Qualifications
Preferred Qualifications
Join Amgens Mission of Serving Patients
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.
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.
Role
Sr Data Management Support
What you will do
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.
- 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 escalate 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
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 6 years of clinical execution experience
Preferred Qualifications
- 3 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