57 matching jobs for “Study Delivery Associate”

How results work

Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.

Amgen

Study Delivery Associate

Hyderabad, India

Full time
Regular

Role Name: Study Delivery Associate ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and …

Added Oct 15, 2026

Save job

Amgen

Study Delivery Associate

Hyderabad, India

Full time
Regular

Role Name: Study Delivery Associate ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and …

Added Oct 15, 2026

Save job

Amgen

Study Delivery Associate

Hyderabad, India 2 postings

Full time
Regular

Role Name: Study Delivery Associate Role GCF: 3 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest …

Added Oct 15, 2026

Save job

Amgen

… 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 …

Added Oct 15, 2026

Save job

Amgen

Study Delivery Sr Associate

Hyderabad, India

Full time
Regular

Job Description: Study Delivery Associate Role Name: Study Delivery Sr Associate Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of biology and …

Added Oct 15, 2026

Save job

Amgen

Study Delivery Sr Associate

Hyderabad, India

Full time
Regular

Job Description: Study Delivery Senior Associate (SDSA) Role Name: Study Delivery Senior Associate Role GCF: 4 ABOUT AMGEN Amgen …

Added Oct 15, 2026

Save job

Amgen

Study Delivery Sr Associate

Hyderabad, India 2 postings

Full time
Regular

Role Name: Study Delivery Senior Associate ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the …

Added Oct 15, 2026

Save job

Amgen

Study Delivery Sr Associate

Hyderabad, India

Full time
Regular

Role Name: Study Delivery Senior Associate Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of biology and technology to …

Added Oct 15, 2026

Save job

Amgen

Mgr Centralized Study Support

Hyderabad, India

Full time
Regular

M anager, Centralized Study Support (CSS) Role Name: Manager Centralized Study Support (CSS) Role GCF: 5 ABOUT AMGEN Amgen harnesses …

Added Oct 15, 2026

Save job

Amgen

Study Data Deliver Mgr

Hyderabad, India

Full time
Regular

… as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Data Delivery Lead What you will do Let’s do this. Let’s change the world. In this vital role you are accountable for the …

Added Oct 15, 2026

Save job

Amgen

Manager Centralized Study Support

Hyderabad, India

Full time
Regular

… Role Description: The Manager, CSS is accountable for hiring, managing, mentoring and growing a team of Study Delivery Associates and Sr Associates. The role is accountable for continually developing the CSS roles …

Added Oct 15, 2026

Save job

Amgen

Sr Mgr Centralized Study Support

Hyderabad, India

Full time
Regular

Role Name: Sr Manager Centralized Study Support (CSS) Role GCF: 6 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the …

Added Oct 15, 2026

Save job

Amgen

Sr Associate Clinical Finish Drug Product Global Study Planner Support

Hyderabad, India

Full time
Regular

… Let’s do this. Let’s change the world. In this vital role, you will serve as lynchpin between Global Study Planners and internal and external customers to ensure supply for our important patients participating in …

Added Oct 15, 2026

Save job

Amgen

Senior Manager Program Data Delivery

Hyderabad, India

Full time
Regular

Role Description: The Program Data Delivery Sr Manager p rovide s program-level oversight and accountability for data delivery across multiple studies, …

Added Oct 15, 2026

Save job

Amgen

Sr Associate Biostatistics

Hyderabad, India

Full time
Regular

… over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Biostatistics Sr Associate What you will do Let’s do this. Let’s change the world. Amgen is expanding its global Biostatistics …

Added Oct 15, 2026

Save job

Amgen

Associate Director Biostatistics

Taipei, Taiwan

Full time
Regular

… is expanding its global Biostatistics capabilities, with Amgen Taiwan playing a key role in integrated delivery and functional leadership. As Associate Director, Biostatistics, you will contribute statistical strategy, …

Added Oct 15, 2026

Save job

Amgen

Database Design Associate

Hyderabad, India

Full time
Regular

… activities across the clinical trial lifecycle, ensuring high-quality, timely, and compliant data delivery to enable effective study outcomes and decision-making. Support execution of core data management …

Added Oct 15, 2026

Save job

Amgen

Biostatistical Programming Associate

Hyderabad, India

Full time
Regular

Biostatistical Programming Associate HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

Save job

Amgen

Biostatistical Programming Associate

Hyderabad, India

Full time
Regular

Biostatistical Programming Associate HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

Save job

Amgen

Biostatistical Programming Senior Associate

Taipei, Taiwan

Full time
Regular

… (JAPAC) is the fastest growing region in Amgen. Now we are hiring a Biostatistical Programming Senior Associate in Taipei, Taiwan. Live What you will do Amgen is expanding its global Biostatistics capabilities, with …

Added Oct 15, 2026

Save job

Amgen

Study Delivery Sr Associate

Hyderabad, India

Full time
Regular

Same role posted 2 times, once per location

View job

Save job

About this opportunity

Original employer description

Career Category

Operations

Job Description

Role Name: Study Delivery Senior Associate

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 Senior Associate provides essential global study management support to clinical study teams, ensuring timely, high-quality, and compliant study execution. They partner with Study Managers to deliver start-up and conduct activities, own specific study tasks and support risk monitoring and issue management, escalating early warning signals with proposed solutions to relevant stakeholders.

The Study Delivery Senior Associate will be assigned to individual study teams and specialize in processes supporting many study teams throughout their study lifecycle, enabling opportunities to gain varied experience in study management.

Roles & Responsibilities:

Study Planning & Coordination

Lead the development and maintenance of study-level trackers, dashboards, timelines, and tools (e.g., vendor management, sample tracking, drug supply planning) to ensure accuracy and visibility.

Coordinate logistics for investigator meetings, trial events, and site communications.

Manage assigned start-up activities, including system setup, access management, and document readiness, ensuring completion to required standards.

Study Execution & Oversight

Use study dashboards and reports to monitor global enrollment, data flow, and quality indicators, taking proactive action to address deviations and risks.

Lead delivery of assigned risk and quality management activities

Track and report study progress, coordinating with Study team and vendors to resolve operational issues and maintain compliance.

Deliver assigned components of global recruitment and retention strategies to help ensure enrollment targets are achieved.

Manage Study Training system activities and oversight

Stakeholder Engagement & Team Collaboration

Build and maintain effective relationships with internal study team members, vendors and investigator sites

Act as a point of contact for routine study updates, ensuring stakeholders are informed and aligned.

Identify, prioritize, and escalate risks effectively to support swift, informed decisions

Site & Vendor Engagement

Lead vendors and supplier set-up to ensure quality, speed, and consistency in deliverables.

Data & Systems Management

Maintain and monitor clinical trial systems (e.g., CTMS), ensuring accurate and timely data entry and reporting.

Support data collection oversight, including query resolution and reconciliation activities.

Manage trial documentation (e.g., TMF) to ensure inspection readiness.

Process Improvement & Knowledge Sharing

Contribute to best practice development, knowledge-sharing and process improvement within the study support community.

Proactively identify and highlight opportunities to streamline / automate activities within remit.

Support Audit/Inspections including Corrective and Preventive Actions (CAPA) processes and embed lessons learned across studies.

Basic Qualifications and Experience:

Master’s degree OR

Bachelor’s degree and 2 years of clinical execution experience OR

Associate’s degree and 6 years of clinical execution experience OR

High school diploma / GED and 8 years of clinical execution experience

Preferred Qualifications and Experience:

3 years’ work experience in life sciences or medically related field, including 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

Competencies:

Strong collaborative and effective communication skills within a team environment.

Understands importance of accuracy in documentation, data tracking, and compliance checks. Identifies discrepancies and escalates appropriately.

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

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

Experience with overseeing vendors and suppliers

Experience executing risk-based site monitoring, Audit and Inspections Corrective and Preventive Actions (CAPA) implementation, and risk mitigation to resolve operational challenges and ensure inspection readiness

Cultural sensitivity and collaboration across global teams.

Ability to recognize, highlight and resolve issues. Demonstrates curiosity and willingness to take on new tasks.

Understanding of the clinical and pharmaceutical drug development process and clinical trial execution principles

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.

Why this result? · Employer labels

All keywords in title

Clinical
Full time
Regular

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.