1,000+ matching jobs for “Clinical Research Associate”

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IQVIA Holdings

Experienced CRA - Real World Evidence with SSU experience

Bucharest, Romania

… of on-site monitoring visits compared with CRA roles supporting traditional interventional or early-phase clinical trials . However, this is balanced by frequent SSU activities, remote site management, regulatory follow-up …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior CRA level II

Prague, Prague, Czechia

… to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage …

Added Oct 16, 2026

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IQVIA Holdings

Director/Senior Director, Business Development, Biotech

London, United Kingdom +8 locations

… european Biotech market, and therefore we are seeking an ambitious individual with a proven track record in clinical sales. The role will be responsible for increasing our client portfolio, and therefore be required to sell …

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Senior CRA I - U.S. Northeast Region - Multiple Therapies

Pittsburgh, Pennsylvania, United States +9 locations

Pay posted by employer$105,000–$112,000

Join Us as Senior Clinical Research Associate I – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical …

Added Oct 29, 2026

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Thermo Fisher Scientific

FSP Sr. CRA I

Remote, California, USA

Pay posted by employer$90,000–$113,000

Join Us as Senior Clinical Research Associate I – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical …

Added Oct 27, 2026

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Thermo Fisher Scientific

Senior/Medical Director (Medical Monitor)

Remote, Malaysia +3 locations 2 postings

Purpose: Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are …

Added Oct 16, 2026

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Thermo Fisher Scientific

Assistant CRA

Belgrade, Central Serbia, Serbia +2 locations 3 postings

Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Nov 3, 2026

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Thermo Fisher Scientific

Assistant CRA

Remote, Spain

Spain: Madrid and Barcelona ONLY Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Thermo Fisher Scientific

Assistant CRA

Remote, Mexico

Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Thermo Fisher Scientific

Assistant CRA

Remote, Romania

Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Amgen

Director, Local Study Operations Manager

United States - Remote

Pay posted by employer$195,876–$265,008

… LSOMs to lead increasingly complex trials and programs. Establishes strong operating partnerships with Clinical Research Associate (CRA) organization to support study start-up, monitoring, issue resolution, and compliant trial execution …

Added Nov 3, 2026

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Amgen

Local Study Operations Line Sr. Manager

United States - Remote

… conditions. 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 Nov 4, 2026

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Merck (MSD)

Principal Scientist, Drug Safety

USA - Pennsylvania - North Wales (Upper Gwynedd)

Pay posted by employer$231,900–$365,000

… CSRM Physician, Principal Scientist, is a physician leader in pharmacovigilance responsible for the overall clinical risk management and safety surveillance of assigned investigational and marketed products. Reporting to a …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sample Coordinator - 1st Shift

Middleton, Wisconsin, United States

… with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and …

Added Oct 16, 2026

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Johnson & Johnson

Sr Mgr Pharma Prod RD

Beerse, Belgium

Full time
Regular

We're hiring a Senior Manager / Associate Director into our Solids Development (SOliD) department within Drug Product Research & Development in …

Added Oct 15, 2026

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Bristol-Myers Squibb

Senior Director, Global Medical Neuroscience, Psychiatry, Mood Disorders

Princeton - NJ - US

Full time
Regular

Pay posted by employer$229,380–$277,956

… while fostering deep cross-functional collaboration with key stakeholders, including US and WW Commercial, Research and Development, Global Drug Development, HEOR, Regulatory Affairs, and global medical stakeholders. The …

Added Oct 15, 2026

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Thermo Fisher Scientific

Sample Coordinator

Singapore, Singapore

Added Oct 27, 2026

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IQVIA Holdings

Site Enrollment & Engagement Lead - National

Parsippany, New Jersey, United States +3 locations

Pay posted by employer$64,400–$195,100

Site Enrollment & Engagement Lead (previously called Clinical Trial Educator) (West, Central, Northeast, Southeast) As a global provider of integrated solutions, IQVIA …

Added Oct 15, 2026

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Pfizer

[R&D] Statistician, バイオメトリクス・データマネジメント統括部　統計担当者

Tokyo, Tokyo, Japan

Full time
Regular

… Provide scientifically rigorous statistical expertise and contributions by working effectively within the clinical triad (clinician, clinical pharmacologist, and statistician) JOB RESPONSIBILITIES Provide scientifically …

Added Oct 16, 2026

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IQVIA Holdings

Lead IT Specialist

Irving, Texas, United States

Pay posted by employer$41,700–$104,200

… and application issues, supporting IT projects, and ensuring high-quality service delivery in a fast-paced clinical environment. In addition to day-to-day technical responsibilities, the Lead IT Specialist helps coordinate …

Added Oct 15, 2026

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IQVIA Holdings

Experienced CRA - Real World Evidence with SSU experience

Bucharest, Romania

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Qualifications · employer excerpt

Bachelor's Degree in a scientific discipline, healthcare or related field preferred.
At least 1 year of independent on-site monitoring experience required.
Previous experience with Site Start-Up activities is strongly preferred, including experience with essential document collection, regulatory/ethics submissions, site activation and follow-up of start-up timelines.
Previous experience in Real World Evidence (RWE), observational, non-interventional, registry or post-authorization studies would be an advantage.
Equivalent combination of education, training and experience may be accepted in lieu of degree.

9 more in the full description below.

About this opportunity

Original employer description

RWE Clinical Research Associate (CRA) with Site Start-Up Experience

Job Overview

Perform monitoring, site management and Site Start-Up (SSU) activities for Real World Evidence (RWE) studies, ensuring that sites conduct studies and report study data in accordance with the study protocol, applicable regulations and guidelines, and sponsor requirements.

The role combines traditional CRA responsibilities with a strong focus on site activation, regulatory and start-up activities. Due to the nature of RWE studies, the position may involve a reduced number of on-site monitoring visits compared with CRA roles supporting traditional interventional or early-phase clinical trials. However, this is balanced by frequent SSU activities, remote site management, regulatory follow-up and coordination across multiple sites, requiring strong organization, prioritization and ownership of a challenging and dynamic workload.

Essential Functions

Perform site monitoring visits, including selection, initiation, monitoring and close-out visits, as required by the study and in accordance with contracted scope of work, applicable regulatory requirements, Good Clinical Practice (GCP), ICH guidelines and sponsor requirements.
Perform and coordinate Site Start-Up activities, including collection and review of essential documents, preparation and follow-up of regulatory and ethics submissions, site activation activities and ongoing communication with investigative sites.
Drive sites through the start-up process, proactively identifying potential delays, following up on outstanding documentation and working with internal and external stakeholders to achieve study timelines.
Manage multiple sites and priorities simultaneously, balancing SSU, monitoring and ongoing site management responsibilities throughout the study lifecycle.
Work with sites to adapt, drive and track subject recruitment plans in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations, milestones and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory and ethics submissions and approvals, site activation, recruitment and enrollment, CRF completion and submission, and data query generation and resolution, as applicable to the study.
Ensure copies/originals, as required, of site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with applicable regulatory and study requirements.
Create and maintain appropriate documentation regarding site management, monitoring activities, visit findings and action plans by submitting regular reports, generating follow-up communications and completing other required study documentation.
Maintain regular remote oversight and communication with assigned sites, ensuring timely follow-up of open actions and study milestones.
Collaborate and liaise closely with study team members, Site Start-Up colleagues, regulatory teams, project management and other functional stakeholders to support successful project execution.
If applicable, support development of project subject recruitment plans on a per-site basis.
If applicable, support site financial management according to executed clinical trial agreements and retrieve invoices according to local requirements.

Qualifications

Bachelor's Degree in a scientific discipline, healthcare or related field preferred.
At least 1 year of independent on-site monitoring experience required.
Previous experience with Site Start-Up activities is strongly preferred, including experience with essential document collection, regulatory/ethics submissions, site activation and follow-up of start-up timelines.
Previous experience in Real World Evidence (RWE), observational, non-interventional, registry or post-authorization studies would be an advantage.
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and ICH guidelines, as applicable to assigned studies.
Good therapeutic and protocol knowledge as provided through company and project-specific training.
Strong organizational and prioritization skills, with the ability to manage a varied workload across multiple sites and different stages of study execution, particularly start-up and ongoing site management activities.
Demonstrated ability to work independently and proactively follow up with investigative sites and internal stakeholders.
Strong problem-solving skills and ability to identify and escalate potential study or site-level risks in a timely manner.
Computer skills including proficiency in Microsoft Word, Excel and PowerPoint and use of relevant clinical research systems and technology.
Strong written and verbal communication skills, including good command of the English language.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, investigative sites and clients.

What to Expect in This Role

This RWE CRA position offers a different balance of responsibilities from a traditional early-phase CRA role. While the number and frequency of on-site monitoring visits may be lower depending on study design and project requirements, the role has a significant Site Start-Up and site management component.

Successful candidates should therefore be comfortable managing frequent site activations, regulatory documentation and follow-up, remote site interactions and multiple concurrent priorities. The position is particularly suited to CRAs who enjoy taking ownership of sites throughout the study lifecycle and who combine solid monitoring experience with strong SSU and organizational capabilities.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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