786 matching jobs for “Senior Clinical Research Associate”

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Thermo Fisher Scientific

(Sr) Clinical Research Associate - Netherlands

Remote, Netherlands

Join Us as a (Senior) Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported …

Added Oct 16, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Early Clinical Development

Carlsbad, California, United States +2 locations

Pay posted by employer$90,200–$175,100

… initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate with site staff to implement and track subject recruitment …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior Clinical Research Associate (Sr CRA)

Remote, Egypt

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

Added Oct 20, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Early Clinical Development

Durham, North Carolina, United States

Pay posted by employer$87,200–$169,300

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate

Remote, Mexico +1 location 3 postings

… 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 20, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate

Remote, Mexico +1 location 4 postings

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate

Remote, North Carolina, USA 2 postings

Sr CRA (Level I) Purpose: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory …

Added Oct 28, 2026

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IQVIA Holdings

(Senior) Clinical Research Associate (CRA)

Hong Kong, Hong Kong +1 location

… initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs …

Added Oct 15, 2026

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IQVIA Holdings

(Senior) Clinical Research Associate (CRA)

Taipei, Taiwan

… and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines • Work with sites to adapt, …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior Clinical Research Associate I

Auckland, Auckland, New Zealand +1 location

… cures for cancer. Location/Division Specific Information Performs and coordinates different aspects of the clinical monitoring and site management process. This home-based position requires candidates to currently be …

Added Oct 25, 2026

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IQVIA Holdings

Clinical Research Associate(Clinical Core)

Seoul, Republic of Korea

… a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: - A Bachelor's degree in a health care or other …

Added Oct 15, 2026

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Thermo Fisher Scientific

Associate Clinical Research Manager

Austin, Texas, United States

Join Us as an Associate Clinical Research Manager - Make an Impact at the Forefront of Innovation The Associate Clinical Research …

Added Oct 25, 2026

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Thermo Fisher Scientific

Clinical Research Associate I

Remote, Singapore

Job Description Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top …

Added Oct 19, 2026

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Abbott Laboratories

Clinical Research Associate II

Alameda, California, United States

Pay posted by employer$81,500–$141,300

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for …

Added Oct 27, 2026

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Abbott Laboratories

Clinical Research Associate I

Alameda, California, United States

Pay posted by employer$73,900–$116,000

Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for …

Added Oct 25, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate I

Vietnam, Vietnam

Job Description Join Us as a Senior 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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Abbott Laboratories

Associate I Clinical Research

Alameda, California, United States

Pay posted by employer$73,900–$116,000

… female executives, and scientists. The Opportunity The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal …

Added Oct 28, 2026

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IQVIA Holdings

Senior Clinical Research Associate - Sponsor Dedicated

Amsterdam, The Netherlands

Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) model …

Added Oct 15, 2026

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IQVIA Holdings

Senior/Clinical Research Associate (Client Dedicated)

Ho Chi Minh City, Vietnam

… with a variety of colleagues and customers . You will need to have a good knowledge of applicable clinical research regulatory requirements. Qualifications: University degree in scientific discipline or healthcare …

Added Oct 15, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Sponsor Dedicated

Carlsbad, California, United States +1 location

Pay posted by employer$74,500–$197,500

Added Oct 15, 2026

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Thermo Fisher Scientific

(Sr) Clinical Research Associate - Netherlands

Remote, Netherlands

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a (Senior) Clinical Research Associate – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

We are seeking CRA's to join our clinical team in The Netherlands. the positions can be office based in Ede, hybrid or fully remote anywhere in NL. We are seeking candidates who already have independent monitoring experience.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a CRA, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
Valid driver's licence where applicable

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manages Risk Based Monitoring concepts and processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Effective interpersonal skills
Strong attention to detail
Effective organizational and time management skills
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Fluency in Dutch and English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Working Conditions and Environment:
Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.
May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.
Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.

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