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We are looking for a talented individual to join us as a Study Designer and Edit Check Programmer, reporting directly to the Sr.
Manager, Clinical Systems and Analytical Reporting.
The successful candidate will play a crucial role in adhering to Amgen standards, procedures, and best practices to build and program studies in our clinical trial database.
This position will require effective partnership with other CSAR Operations and cross-functional staff to ensure seamless, high-quality deliverables and activities related to the use of electronic data capture technology.
We are seeking a strong leader who can confidently influence stakeholders and contribute individually to study-specific and general CSAR/GDO projects or operational work.
The ideal candidate will have proven experience in partnering effectively with cross-functional teams to deliver systems support and study deliverables.
Additionally, they should have operational experience with clinical database management systems and allied technologies (e.g., Rave EDC, Veeva EDC).
At Amgen, if you feel like you’re part of something bigger, it’s because you are.
Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s 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, you’ll 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, you’ll thrive as part of the Amgen team.
Join us and transform the lives of patients while transforming your career.
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We are looking for a talented individual to join us as a Study Designer and Edit Check Programmer, reporting directly to the Sr.
Manager, Clinical Systems and Analytical Reporting.
The successful candidate will play a crucial role in adhering to Amgen standards, procedures, and best practices to build and program studies in our clinical trial database.
This position will require effective partnership with other CSAR Operations and cross-functional staff to ensure seamless, high-quality deliverables and activities related to the use of electronic data capture technology.
We are seeking a strong leader who can confidently influence stakeholders and contribute individually to study-specific and general CSAR/GDO projects or operational work.
The ideal candidate will have proven experience in partnering effectively with cross-functional teams to deliver systems support and study deliverables.
Additionally, they should have operational experience with clinical database management systems and allied technologies (e.g., Rave EDC, Veeva EDC).
include, but are not limited to, the following:
Amgen is a global biotechnology company that discovers, develops, manufactures and delivers innovative medicines for serious diseases, including cancer, heart disease, inflammatory conditions and rare diseases.
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Senior · 12+ years experience
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