Amgen - India, On-site work

Join a leading clinical research team as a Study Delivery Sr Associate in Hyderabad, India. Support global trial management by maintaining trackers, ensuring regulatory compliance, and coordinating study start-up activities. Ideal candidates bring a Bachelor’s degree or equivalent clinical execut...

Amgen seeks a Data Delivery Lead in Hyderabad, India, to drive study-level data management for global clinical trials. You will lead data management plans, oversee database build and UAT, and ensure on-time delivery through proactive metric monitoring. Requires 8-15 years’ life sciences experienc...

Lead the acquisition and quality management of non-CRF clinical trial data as Data Acquisition Lead in Hyderabad, India. This role requires 8+ years of clinical execution experience, including vendor oversight and global trial delivery. You will ensure timely, compliant data ingestion, drive auto...

Study Delivery Senior Associate needed in Hyderabad, India to support global clinical trial execution. You will partner with Study Managers, lead study trackers, dashboards, and vendor logistics while managing start-up activities and risk monitoring. Requires a Master’s degree or equivalent clini...

Join Amgen in Hyderabad as a Regulatory Statistical Programming expert. Leverage your SAS, R, or Databricks skills to support real-world evidence (RWE) generation for regulatory submissions. Ideal for professionals with a Bachelor’s in a scientific field and 2+ years of life sciences programming ...

Seeking a **Study Data Delivery Manager** in **Hyderabad, India** to lead end-to-end clinical data management. You will ensure high-quality, decision-ready data by driving the Data Management Plan, overseeing database build, and managing study conduct activities. Ideal candidates have a life scie...

Lead C&Q documentation preparation for Drug Product systems at Amgen in Hyderabad. This role requires 8-13 years of GMP commissioning and qualification experience in pharma or biotech. You will manage a blended team, overseeing protocols, risk assessments, and traceability matrices for global Eng...

Lead C&Q documentation preparation for Finished Drug Product and packaging systems at Amgen in Hyderabad. This role manages a blended team, ensuring compliant, inspection-ready protocols and reports for GMP manufacturing and capital projects. Requires 8-13 years in pharmaceutical commissioning/qu...

Seeking a skilled Reltio MDM Developer to join us as Associate, Data Management in Hyderabad. You will design scalable MDM solutions, leveraging expertise in Lifecycle Actions (LCA), Java, and API integrations. Ideal candidates have 2-5 years of experience, strong SQL/Python skills, and Pharma/Li...

Lead C&Q documentation for major biotech projects in Hyderabad. Manage a team preparing GMP qualification protocols and reports for drug substance manufacturing systems. Requires 8+ years in pharma validation and strong leadership experience. Ensure compliance and operational readiness in a dynam...

Lead C&Q documentation for pharmaceutical facilities and utilities at Amgen's Hyderabad site. Manage a team preparing compliant, inspection-ready protocols and reports. Requires 8+ years in GMP commissioning/qualification and team leadership. Ensure project success in a dynamic, cross-functional ...

Senior Associate Supply Chain Compliance Management role in Hyderabad, India. Ensure GMP compliance, manage SOPs, and lead documentation for Amgen's external manufacturing network. Requires 5-9 years' supply chain experience in pharma/biotech, strong GMP knowledge, and audit support skills. Drive...