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

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Thermo Fisher Scientific

CRA (Level I) - FSP

Remote, Chile

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active …

Added Oct 16, 2026

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IQVIA Holdings

Analyst - Assoc Consultant, Real World Solutions (Epidemiologist)

Taipei, Taiwan +2 locations

… and generation of evidence around key epidemiological features for real world studies Perform desk research, literature reviews and data analysis Work closely with various project team members including project …

Added Oct 15, 2026

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Amgen

Sr Mgr Centralized Study Support

India - Hyderabad

Full time
Regular

… Study Support (CSS). This role ensures delivery of high ‑ quality centralized operational support across clinical programs and alignment of resources with organizational priorities. Roles & Responsibilities: Team …

Added Oct 15, 2026

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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

Scientist I, Biopharma, Morning, Core or Evening Shift - Athlone, Ireland

Athlone, Leinster, Ireland

… 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 Nov 6, 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 +1 location 2 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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Thermo Fisher Scientific

Sample Coordinator - 1st Shift

Middleton, Wisconsin, United States

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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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

CRA (Level I) - FSP

Remote, Chile

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Experience and skills · employer excerpt

This role typically requires 0 - 2 years of prior relevant experience. Good knowledge of clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).…
Degree in scientific discipline or health care. Equivalent combination of education, training and experience may be accepted in lieu of degree.

About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team / local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.

The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

A CRA with longer tenure and experience may take on additional responsibilities that include additional tasks associated with LSAD.

CRAs might have different internal titles based on the experience level (CRA, Senior CRA). The experience level depends on the years of experience, performance record, level of independence in the role, ability to take on additional tasks or tutor more junior colleagues. The Country Head may assign this internal title after confirmation with Senior Director, Cluster Head or Executive Director, Regional Head.

Typical Accountabilities

Contributes to the selection of potential investigators.
In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process, submission of proper applications/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
Trains, supports and advises investigators and site staff in study related matters, including Risk Based Quality Management (RBQM) principles.
Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
Actively participates in local Study Team (LST) meetings.
Contributes to National Investigators meetings, as applicable.
Initiates, monitors and closes study sites in compliance with AZ Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate.
Updates CTMS and other systems with data from study sites as per required timelines.
Manages study supplies (e.g. etc), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
Performs monitoring visits (remote and on-site), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines and discusses with LSAD the correct timing and type of visits.
Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
Ensures data query resolution in a timely manner.
Works with data management to ensure robust quality of the collected study data.
Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
Prepares and finalises monitoring visit reports in CTMS and provides timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with AZ SOP.
Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, CSP or ICH-GCP compliance issues to Local Management and/or CQM as required.
Assists site in maintaining inspection ready ISF.
Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and CQAD.
Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, AZ SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of the local part of the eTMF.
Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
Ensures compliance with AstraZeneca's Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).
Ensures compliance with local, national and regional legislation, as applicable.
Collaborates with local MSLs as directed by LSAD or line manager.

Experience and skills

This role typically requires 0 - 2 years of prior relevant experience. Good knowledge of clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Written and verbal communication skills including good command of English language.

Degree in scientific discipline or health care. Equivalent combination of education, training and experience may be accepted in lieu of degree.

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