Amgen Careers has announced a new opportunity for the role of Study Delivery Associate in Hyderabad, India. This clinical research job is ideal for candidates with experience in clinical trial operations, CTMS, eTMF, study coordination, and biotech clinical research.
Candidates from life sciences backgrounds looking to build careers in clinical operations, study management, and global clinical trials can apply for this Amgen clinical research opening.
About Amgen
Amgen Official Website is one of the worldโs leading biotechnology companies focused on discovering and developing innovative medicines for serious illnesses. The company operates globally and is known for advancements in biologics, oncology, inflammation, cardiovascular diseases, and rare diseases.
Job Details
| Particulars | Details |
|---|---|
| Job Title | Study Delivery Associate |
| Company | Amgen |
| Location | Hyderabad |
| Department | Clinical Development |
| Job Type | Full-Time |
| Work Mode | On Site |
| Experience Required | 1โ2 Years Preferred |
| Qualification | Bachelorโs Degree in Life Sciences or related field |
| Industry | Biotechnology / Clinical Research / CRO |
Key Responsibilities of Study Delivery Associate
The Study Delivery Associate will support clinical trial management and operational activities across global studies. Key responsibilities include:
- Supporting study timelines, dashboards, trackers, and study coordination activities
- Assisting in clinical trial documentation and regulatory submissions
- Managing CTMS, eTMF, and study-related systems
- Supporting study start-up activities and investigator meeting logistics
- Coordinating investigational product logistics and biological sample management
- Assisting with trial risk management and quality review documentation
- Supporting inspection readiness and regulatory compliance activities
- Maintaining accurate clinical trial data entry and system updates
- Supporting vendor coordination and site engagement activities
- Ensuring protocol adherence and document version control
Required Qualifications
Basic Qualifications
Candidates should possess one of the following:
- Bachelorโs Degree in Life Sciences or related field
OR - Associate degree with 4 years of clinical execution experience
OR - High school diploma/GED with 6 years of clinical execution experience
Preferred Qualifications
- 1โ2 years of experience in clinical research or biotech/pharmaceutical industry
- Experience working on global clinical trials
- Knowledge of CTMS, eTMF, EDC systems
- Familiarity with clinical trial documentation and regulatory processes
- Strong MS Excel, Word, and PowerPoint skills
- Good communication and cross-functional collaboration abilities
Skills Required
Candidates applying for this clinical research job in Hyderabad should have:
- Clinical trial operations knowledge
- CTMS and eTMF experience
- Regulatory documentation handling
- Study coordination skills
- Data management and tracking abilities
- Problem-solving mindset
- Knowledge of GCP and inspection readiness
- Vendor and site coordination experience
Salary and Benefits
The estimated salary for the Amgen Study Delivery Associate role in Hyderabad is approximately:
- โน5.5 LPA โ โน9 LPA (Estimated based on industry standards)
Employee Benefits
- Opportunity to work on global clinical trials
- Exposure to biotech clinical development programs
- Career growth in clinical operations
- Learning and development programs
- International work culture
- Health and wellness benefits
Why Join Amgen?
Amgen offers professionals an opportunity to work in a highly innovative biotechnology environment with global exposure in clinical development and study delivery. Candidates interested in clinical operations jobs, CTMS jobs, and clinical trial associate careers can gain strong industry experience through this role.
How to Apply
