Hyderabad Telangana Senior clinical data associate Jobs – 62 Open Jobs Today

Study Delivery Sr Associate
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
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Mgr Data Management Support
Amgen —Hyderabad, Telangana
- Microsoft Excel
- Master's degree
- 12th Pass
Biostatistics Sr Assoc (Study Statistician)
Amgen —Hyderabad, Telangana
- Doctoral degree
- English
- Master's degree
Senior Manager, Scientific and Operations Intelligence - Obesity
Amgen —Hyderabad, Telangana
- Master's degree
- Analysis skills
- Bachelor's degree
Analyst II, FP&A Commercialization Markets
Bristol-Myers Squibb —Hyderabad, Telangana
- Email
- Hybrid work
- Analysis skills
- Travel
Senior Project Manager RTSM - Operations
Signant Health —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- PMP
Senior Associate - RWE Application Development
Amgen —Hyderabad, Telangana
- Computer Science
- English
- Java
Medical Review Senior Associate Scientist
Amgen —Hyderabad, Telangana
- Medicine
Sr Associate Clinical Finish Drug Product Global Study Planner Support
Amgen —Hyderabad, Telangana
- ERP systems
- English
- Master's degree
Senior Associate - RWE Obesity Statistical Programming
Amgen —Hyderabad, Telangana
- Computer Science
- English
- Master's degree
Sr Associate Clinical Supply Chain Support Office
Amgen —Hyderabad, Telangana
- Microsoft Word
- English
- Microsoft Office
Sr Associate, Web Strategy & Operations
Amgen —Hyderabad, Telangana
- Doctoral degree
- English
- Research
Associate Solutions Designer
Perceptive —Hyderabad, Telangana
- Full-time
- English
- Bachelor's degree
- Communication skills
10d
Sr Associate Biostatistics
Amgen —Hyderabad, Telangana
- Doctoral degree
- English
- Master's degree
Manager - TA Access Early Assets-2
Novartis —Hyderabad, Telangana
- Full-time
- Microsoft Word
- Microsoft Excel
- Doctoral degree
Manager - TA Access Early Assets-1
Novartis —Hyderabad, Telangana
- Full-time
- Microsoft Word
- Microsoft Excel
- Doctoral degree
Program Officer, AI Access Initiative (EAII Advisors)
Evidence Action —Hyderabad, Telangana
- English
- Microsoft Office
- Master's degree
- Health insurance
- Life insurance
Quick apply
Business Development Manager Supply Chain AXP
Amgen —Hyderabad, Telangana
- Management
- Master's degree
- Bachelor's degree
Sr. Associate Systems Analyst
Amgen —Hyderabad, Telangana
- Evening shift
- DevOps
- Master's degree
- SQL
Database Design Sr Associate
Amgen —Hyderabad, Telangana
- Computer Science
- Microsoft Office
- Master's degree

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Study Delivery Sr Associate

Amgen -
Hyderabad, Telangana

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Job details

Qualifications

Microsoft Powerpoint
Microsoft Word
Clinical research
Filing
Process improvement
Research
Microsoft Office
12th Pass
Bachelor's degree
Data management
Clinical trials

Full job description

India - Hyderabad

JOB ID: R-238190 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jul. 10, 2026 CATEGORY: Clinical

Job Description:

Study Delivery Associate

Role Name:Study Delivery Sr Associate

Role GCF: 4

ABOUT AMGEN

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier,fullerand longer. We discover, develop,manufactureand deliver innovative medicines to help millions of patients. Amgen helpedestablishthe biotechnology industry more than 40 years ago andremainson thecutting-edgeof innovation, using technology and human genetic data to push beyondwhat’sknown 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 DeliveryTeam in meeting study timelines, ensuring regulatory compliance, and executing standardized processes related to clinical trial coordination,documentand system management.

TheStudy DeliveryAssociatemayalsosupportspecializedactivities to promoteexpertise, quality, and consistency across studies. Key responsibilities includemaintainingaccurateandtimelydata 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,dashboardsand timelines.

Communicate study progress,timelinesand deliverables to the Study Delivery Manager.

Assistwith tracking and following up on study actions, including risk mitigation actions.

Assistwith the preparation and record keeping of risk & quality reviews.

Ensure completion of study team training andinspectionreadiness activities tomaintaincompliance with regulatory requirements.

Assistwith trial-related events, global site communications, andlogisticsfor 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,reconciliationand analysis of biological samples.

Coordinate investigational productlogistics, ensuring compliance with reconciliation processes.

Data & Systems Management

Maintain clinical trial systems (e.g., CTMS, study training), ensuringtimelyandaccuratedata entry.

Support system access requests and access management.

Document Preparation

Assistwith preparing,reviewingandmaintainingstudy documentation, including regulatory submissions, monitoringplansand study guides.

Support TMF filing.

Process Improvement & Knowledge Sharing

Contribute to process improvement and share knowledge& shareknowledge 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

PreferredQualifications 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:

Expertisein 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 withtracking and filingof 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 tomaintainaccurateandtimelydata 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,highlightand 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 toparticipatein the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to requestan accommodation.

Apply Now

Refine Your Search

senior clinical data associate jobs in hyderabad telangana

Study Delivery Sr Associate

Mgr Data Management Support

Biostatistics Sr Assoc (Study Statistician)

Senior Manager, Scientific and Operations Intelligence - Obesity

Analyst II, FP&A Commercialization Markets

Senior Project Manager RTSM - Operations

Senior Associate - RWE Application Development

Medical Review Senior Associate Scientist

Sr Associate Clinical Finish Drug Product Global Study Planner Support

Senior Associate - RWE Obesity Statistical Programming

Sr Associate Clinical Supply Chain Support Office

Sr Associate, Web Strategy & Operations

Associate Solutions Designer

Sr Associate Biostatistics

Manager - TA Access Early Assets-2

Manager - TA Access Early Assets-1

Program Officer, AI Access Initiative (EAII Advisors)

Business Development Manager Supply Chain AXP

Sr. Associate Systems Analyst

Database Design Sr Associate

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