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Data Acquisition Mgr

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Amgen

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Location:
India , Hyderabad

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Category:
IT - Software Development

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

Join Amgen’s Mission of Serving Patients. 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.

Job Responsibility:

  • Lead the acquisition, integration, and quality management of non-CRF (external/vendor) clinical trial data
  • Own the design, setup, and ongoing management of non-CRF data (e.g., central labs, imaging, wearables, precision medicine)
  • Own, define and maintain vendor data transfer specifications
  • Ensure timely and accurate ingestion of external datasets
  • Partner with other Data Management roles to ensure external data aligns with CRF structures
  • Lead troubleshooting of vendor integration issues
  • Monitor the quality of incoming data throughout the study lifecycle

Requirements:

  • Master’s degree and 8 years of clinical execution experience OR Bachelor’s degree and 8 years of clinical execution experience
  • 8 years’ work experience in life sciences or medically related field, including 3 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials
  • Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)

Additional Information:

Job Posted:
May 06, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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