Clinical Research Job at Amgen | Life Sciences | Apply Now
Amgen, one of the world’s leading biotechnology companies, is hiring for a Study Delivery Associate position at its capability center in Hyderabad. This clinical research job is a specialized operational role that supports the execution of global clinical trials, ensuring they remain on schedule and compliant with international regulatory standards. An Amgen career offers the chance to work at the forefront of human genetics and innovative drug development. As a pioneer in the industry for over 40 years, Amgen integrates biology and technology to treat the world’s toughest diseases.
- Job Position: Study Delivery Associate
- Location: Hyderabad, India
- Job ID: R-232833
- Category: Clinical Development
About the Company
Amgen is a global biotechnology powerhouse focused on six therapeutic areas: oncology/hematology, cardiovascular disease, inflammation, bone health, nephrology, and neuroscience. With a presence in over 100 countries, Amgen’s Hyderabad site is a vital hub for global trial operations. Amgen uses large-scale human genetic data to “push beyond what’s known today,” making it a premier destination for those seeking an Amgen career.
Job Overview
The Study Delivery Associate provides critical administrative and technical support to the Study Delivery Team. This role is central to maintaining the “Inspection Readiness” of a trial through meticulous document control and systems management.
Key Responsibilities:
- Study Coordination: Setup and maintain study-level trackers, dashboards, and timelines. You will assist in tracking risk mitigation actions and ensuring all team members complete mandatory training.
- Logistics & Supply Chain: Manage the shipment and reconciliation of biological samples and coordinate investigational product (IP) logistics.
- Systems Management: Maintain accurate data entry in the Clinical Trial Management System (CTMS) and manage access requests for various study platforms.
- Documentation: Assist in preparing and reviewing regulatory submissions, monitoring plans, and study guides. You will also be responsible for filing essential documents in the Trial Master File (TMF).
Qualifications & Experience
To qualify for this clinical research job, Amgen requires a combination of education and industry-specific experience:
- Basic Requirements: * Bachelor’s degree OR
- Associate’s degree with 4 years of clinical execution experience OR
- High school diploma with 6 years of experience.
- Preferred Profile: 2 years of work experience in life sciences, including at least 1 year of biopharmaceutical clinical research experience at a biotech, pharma, or CRO.
- Technical Skills: Working knowledge of CTMS, eTMF, and EDC (Electronic Data Capture) systems.
Securing a clinical research job at Amgen’s Hyderabad facility is a high-impact move for professionals dedicated to the operational side of drug development. This role provides deep exposure to global trial trackers, regulatory documentation, and bio-sample logistics. By advancing your Amgen career, you contribute to a legacy of innovation that has defined the biotechnology industry for four decades. If you have experience with CTMS/eTMF and a Bachelor’s degree in Life Sciences, apply for the Job today.
