Study Delivery Associate
Amgen
Amgen is hiring talented professionals for the position of Study Delivery Associate in India - Hyderabad. This opportunity is ideal for candidates looking to build a strong career in the IT industry in 2026. Applicants should carefully review the eligibility criteria, required skills, and selection process before applying online.
The recruitment drive for 2026 offers a great chance for job seekers to join a reputed organization. Make sure to prepare well for the interview and submit your application before the deadline. Read below for full details on how to apply, educational qualifications, and other important instructions.
Job Overview
| Role: | Study Delivery Associate |
| Location: | India - Hyderabad |
| Employment Type: | Full Time / Permanent |
| Industry: | IT / Software / Core |
🚀 Why Study Delivery Associate is a Strategic Career Move in 2026
Joining Amgen as a Study Delivery Associate offers excellent growth prospects. Here's why this role is trending:
- Networking on LinkedIn can open doors to unadvertised opportunities.
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Industry Insight: General roles in India - Hyderabad are currently seeing high demand.
Organization / Company Name
Amgen
(See full description for company details)
🎯 How to Prepare for Study Delivery Associate Role
To crack the interview at Amgen, focus on the following:
- Mock interviews can significantly boost your confidence.
- Prepare answers for common behavioral questions (STAR method).
- Research the company's culture and values before the interview.
Important Dates
- Posted On: 20 March 2026
- Application Deadline: ASAP (Apply immediately)
Job Description
Career Category
ResearchJob Description
Role Name: Study Delivery Associate
Role GCF: 3
ABOUT AMGEN
Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.
ABOUT THE ROLE
Role Description:
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.
Roles & Responsibilities:
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 & share knowledge and experience.
Basic Qualifications and Experience:
- 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
Preferred Qualifications and Experience:
2 years' work experience in life sciences or medically related field, including 1 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company Experience working on global clinical trials
Competencies:
- Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
- Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support
- Experience with tracking and filing of essential documents such as protocols, informed consent forms, and regulatory submissions to ensure documents are version-controlled and inspection-ready.
- 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 recognize, highlight and resolve issues. Demonstrates curiosity and willingness to take on new tasks.
EQUAL OPPORTUNITY STATEMENT
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
.Educational Qualification
Candidates should possess a relevant degree (B.E/B.Tech, M.E/M.Tech, MCA, or equivalent) from a recognized university. Please refer to the specific requirements in the Job Description above.
Age Limit
As per company rules. Generally, candidates should be at least 18 years of age.
Salary / Pay Scale
Best in Industry / Not Disclosed by Company.
Application Fee
NIL (No application fee for private jobs).
Selection Process
- Resume Shortlisting
- Online Assessment / Technical Round
- HR Interview
- (Process may vary by company)
How to Apply
Interested and eligible candidates can apply online using the link provided below.
- Click on the "Apply Now" link below.
- You will be redirected to the official career page of Amgen.
- Read the job details carefully.
- Click on "Apply" and fill in the required details.
- Submit your application.
Important Links
Important Instructions
- Read the full job description on the official site before applying.
- Ensure your resume is updated and matches the job requirements.
- Check your email regularly for updates after applying.
Kishan Prajapati
Career Researcher & IT Industry Analyst. Helping freshers and professionals find verified private IT job opportunities in India.
Disclaimer: This job posting is for information purposes only. We are not associated with Amgen directly. All applications are processed through the official company website. Do not pay any money to anyone for this job.
