749 matching jobs for “Senior Clinical Research Associate”

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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 Sr Associate

India - Hyderabad 2 postings

Full time
Regular

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

Added Oct 15, 2026

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IQVIA Holdings

… • Ability to work under time constraints and changing work volumes. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare …

Added Oct 16, 2026

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Amgen

Study Delivery Sr Associate

India - Hyderabad

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

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Amgen

Senior Associate Biostatistical Programming

Taipei, Taiwan, Taiwan

Full time
Regular

Senior Associate Biostatistical Programming (Taipei, Taiwan) HOW MIGHT YOU DEFY IMAGINATION? Amgen is one of the …

Added Oct 15, 2026

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Amgen

Senior Associate Biostatistical Programming

Taipei, Taiwan, Taiwan

Full time
Regular

Senior Associate Biostatistical Programming (Taipei, Taiwan) HOW MIGHT YOU DEFY IMAGINATION? Amgen is one of the …

Added Oct 15, 2026

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IQVIA Holdings

Senior Site Contracts Associate

Mexico City, Mexico

IQVIA Biotech is hiring for Sr. Site Contracts Associate in Mexico with 5 years experience negotiating clinical site contracts and budget templates. Must have CRO, …

Added Oct 15, 2026

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IQVIA Holdings

Senior Site Contracts Associate

São Paulo, Brazil

IQVIA Biotech is hiring for Sr. Site Contracts Associate in Brazil with 5 years experience negotiating clinical site contracts and budget templates. IQVIA Biotech …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate

Taipei, Taiwan, Taiwan

Full time
Regular

… Asia Pacific (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 …

Added Oct 15, 2026

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Johnson & Johnson

Snr Clinical & Sales Specialist

North Ryde, New South Wales, Australia

Full time
Regular

… on their journey to wellness. The Opportunity An opportunity has become available for a results driven Senior Clinical Specialist to join our Electrophysiology Team in Sydney . The overall responsibility of this role …

Added Oct 15, 2026

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Amgen

Process Development Senior Associate

Thousand Oaks, California, United States

Full time
Regular

… cancer. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our …

Added Oct 15, 2026

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Amgen

Senior Associate Medical Data Reviewer

India - Hyderabad

Full time
Regular

In this vital role, the Senior Associate - Medical Data Reviewer is responsible for ensuring the clinical integrity, quality, and …

Added Oct 15, 2026

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Amgen

Database Design Sr Associate

India - Hyderabad

Full time
Regular

… technology and human genetic data to push beyond what’s known today. ABOUT THE ROLE Role Description: The Senior Database Designer is responsible for translating study protocol requirements into compliant, scalable, and …

Added Oct 15, 2026

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Amgen

Data Management Sr Associate

India - Hyderabad

Full time
Regular

… each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our …

Added Oct 15, 2026

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Amgen

Sr Associate Transactional Finance

India - Hyderabad

Full time
Regular

Job Description Amgen’s Research and Development (R&D) Business Operations organization addresses complex business challenges with …

Added Oct 15, 2026

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Amgen

Biostatistics Sr Associate – Data Visualization

India - Hyderabad

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

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Regeneron Pharmaceuticals

Sr. Associate Scientist-1

Hyderabad, Telangana, India

Full time
Regular

… and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Associate Scientist I, PM - Quantitative Biomarker Sciences to join our team in Hyderabad. In this role, …

Added Oct 30, 2026

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Pfizer

SOQ HUB Senior Associate

Makati City, National Capital Region, Philippines

Full time
Regular

… always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. What You Will Achieve In this role, you will: …

Added Oct 16, 2026

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Gilead Sciences

Sr Associate Scientist, Biology

Foster City, California, United States

Full time
Regular

Pay posted by employer$126,820–$164,120

We are seeking a highly motivated Senior Associate Scientist to join the Research Oncology group and contribute to the discovery and development of …

Added Oct 15, 2026

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Pfizer

Senior Associate - Downstream Validation

Visakhapatnam, Andhra Pradesh, India

Full time
Regular

Why Patients Need You Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and …

Added Oct 16, 2026

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Amgen

Senior Associate - Strategic Planning & Operations

India - Hyderabad

Full time
Regular

Job Description Increasing demand for observational research (now commonly referred to as real-world evidence [RWE]) from regulatory and reimbursement authorities makes …

Added Oct 15, 2026

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Amgen

Study Delivery Sr Associate

India - Hyderabad

Full time
Regular

Same role posted 2 times, once per location

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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.

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Keywords also found in description

Clinical
Full time
Regular

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