Life Science Jobs at Amgen | Candidates Apply Now
Are you looking for Life Science Jobs in Clinical Research? Here’s an excellent opportunity to build your career with Amgen Careers. Amgen is hiring for the Study Delivery Associate position in Hyderabad. Candidates with a Bachelor’s degree and experience in clinical research, biotechnology, pharmaceuticals, or CRO environments can apply. If you are searching for Clinical Research Jobs and want to work with a global biotechnology leader, this opportunity is worth exploring.
About Amgen
Amgen is a global biotechnology company that harnesses the power of biology and technology to fight the world’s toughest diseases. For more than 40 years, Amgen has been discovering, developing, manufacturing, and delivering innovative medicines that improve the lives of millions of patients worldwide. The company continues to lead the biotechnology industry by leveraging cutting-edge science, advanced technology, and human genetic data to drive medical innovation. Amgen Careers provide excellent opportunities for professionals seeking rewarding Life Science Jobs and Clinical Research Jobs in a collaborative and innovation-driven environment.
Job Details
- Position: Study Delivery Associate
- Job ID: R-241470
- Location: Hyderabad, India
- Work Type: On-Site
- Category: Clinical Development
Key Responsibilities
The Study Delivery Associate provides essential administrative and operational support to clinical trial management activities. This role supports the Study Delivery Team in meeting study timelines, ensuring regulatory compliance, and executing standardized processes related to clinical trial coordination, document and system management.
The Study Delivery Associate may also support specialized activities to promote expertise, quality, and consistency across studies. Key responsibilities include maintaining accurate and timely data within clinical systems (e.g., CTMS) and supporting study training and related operational requirements.
Study Coordination
- Support the setup and maintenance of study-level trackers, dashboards and timelines.
- Communicate study progress, timelines and deliverables to the Study Delivery Manager.
- Assist with tracking and following up on study actions, including risk mitigation actions.
- Assist with the preparation and record-keeping of risk & quality reviews.
- Ensure completion of study team training and inspection readiness activities to maintain compliance with regulatory requirements.
- Assist with trial-related events, global site communications, and logistics for investigator meetings.
- Support study start-up activities, including system setup, supplier access management, ICF tracking and document readiness.
- Support vendor relationships and site engagement strategies.
- Manage shipment, reconciliation and analysis of biological samples.
- Coordinate investigational product logistics, ensuring compliance with reconciliation processes.
Data & Systems Management
- Maintain clinical trial systems (e.g., CTMS, study training), ensuring timely and accurate data entry.
- Support system access requests and access management.
Document Preparation
- Assist with preparing, reviewing and maintaining study documentation, including regulatory submissions, monitoring plans and study guides.
- Support TMF filing.
Process Improvement & Knowledge Sharing
- Contribute to process improvement and share knowledge and experience.
Qualifications
Basic Qualifications
- Bachelor’s degree OR
- Associate’s degree and 4 years of clinical execution experience OR
- High school diploma / GED and 6 years of clinical execution experience.
Experience
Preferred Experience
- 2 years’ work experience in life sciences or a medically related field.
- 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company.
- Experience working on global clinical trials.
Skills Needed
- Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organisation environments.
- Strong skills in MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support.
- Experience with tracking and filing essential documents such as protocols, informed consent forms, and regulatory submissions.
- Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools.
- Ability to maintain accurate and timely data entry.
- Skilled in managing clinical trial data flow, investigator documentation, and protocol adherence while ensuring regulatory compliance.
- Cultural sensitivity and collaboration across global teams.
- Ability to recognise, highlight and resolve issues.
- Demonstrates curiosity and willingness to take on new tasks.
If you’re searching for Life Science Jobs, Amgen Careers, or Clinical Research Jobs, this Study Delivery Associate opportunity in Hyderabad offers an excellent chance to work with one of the world’s leading biotechnology companies while contributing to global clinical trials and innovative healthcare solutions.
