Amgen Hiring Study Delivery Associate - Clinical Operations: Hyderabad
Are you seeking rewarding clinical support vacancies via Amgen Careers Hyderabad or Study Delivery Associate Jobs? Global biotechnology pioneer Amgen is inviting applications for the position of Study Delivery Associate at its site in Hyderabad.
This role provides administrative and operational support to global clinical trial management activities. It is ideal for candidates with 1 to 2+ years of experience in Trial Master File (TMF) coordination, electronic database trackers (CTMS/eTMF), and study start-up logistics. To draft an optimized resume for biopharma screening, read our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Amgen (Amgen Technology Pvt Ltd) |
| Position | Study Delivery Associate |
| Job Location | Hyderabad, India (On-Site) |
| Employment Type | Full-Time |
| Experience Required | Preferred 1–2+ Years Clinical Trial / Research experience |
| Qualifications | Bachelor's Degree or equivalent clinical execution experience |
| Estimated Salary | ₹8.0 LPA – ₹13.5 LPA (Depending on profile) |
| Ref ID | R-241470 |
💼 Key Responsibilities
- Provide essential administrative and operational support to clinical trial management teams.
- Support setup and maintenance of study-level trackers, operational dashboards, and milestones.
- Communicate study progress, timelines, and action deliverables to the Study Delivery Manager.
- Assist in tracking and following up on risk mitigation plans and quality reviews.
- Ensure complete compliance of study team training records and support inspection readiness tasks.
- Assist with trial-related logistics, investigator meetings, and global site communications.
- Support study start-up activities, including supplier access management, ICF tracking, and document readiness.
- Maintain and update data entries inside Clinical Trial Management Systems (CTMS) and study files.
- Assist with preparing, filing, and reviewing study documentation, including regulatory filings and TMF records.
- Manage shipment, tracking, reconciliation, and analysis coordination of biological samples and investigational products.
To learn how clinical operations and study associate compensation packages scale internationally compared to safety analyst fields, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Experience
Minimum Qualifications:
- Bachelor's degree OR Associate's degree with 4 years of clinical execution experience OR High School Diploma/GED with 6 years of clinical execution experience.
Preferred Qualifications:
- 2 years of work experience in life sciences or medically related fields.
- 1 year or more of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical, or CRO company.
- Prior experience working on global clinical trials.
Required Technical Competencies:
- Proficiency with Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), and electronic Trial Master Files (eTMF).
- Strong skills in MS Word, Excel, and PowerPoint for data management and trial support.
- Experience version-controlling and filing essential documents (protocols, informed consent forms, regulatory letters).
- Strong cultural sensitivity and ability to collaborate across global virtual study teams.
For pharmacy graduates weighing clinical trial execution careers against lab research pathways, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Benefits of Joining Amgen
- Work with a leading pioneer in biotechnology and human genetics therapies.
- Direct exposure to global clinical trials, advanced CTMS platforms, and regulatory compliance standards.
- Highly collaborative environment with continuous professional development programs.
- State-of-the-art office facilities located in the biopharma hub of Hyderabad.
To evaluate your knowledge of clinical trial operations, GCP compliance, and document versioning, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Clinical Operations vs Healthcare IT
Study delivery associates facilitate trial trackers, SOP compliance, and site communication, whereas healthcare informatics supports system architectures. To understand the differences, read our comparison on Healthcare IT vs Clinical Healthcare.
🚀 How to Apply?
Interested and eligible candidates can submit their applications online directly on the official Amgen Workday portal. Click the button below to submit your CV:
Apply Online - Amgen Workday Portal❓ Frequently Asked Questions
Q. What is the required experience for this Study Delivery Associate role?
Amgen prefers candidates with at least 1-2 years of clinical research experience, ideally in a biotech, CRO, or pharmaceutical company.
Q. Where will this role be based?
This is a full-time, on-site role located at Amgen's site in Hyderabad, India.
Q. Which databases and tools are relevant for this position?
Experience with CTMS, eTMF, Electronic Data Capture (EDC), and Microsoft Office (Excel, Word) is preferred.
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