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

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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 50 pharmaceutical …

Added Oct 19, 2026

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IQVIA Holdings

(Senior) Clinical Research Associate

Durham, North Carolina, United States +3 locations 2 postings

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

… to manage multiple priorities in a fast-paced environment Why Join Us Make a direct impact on advancing clinical research and improving patient outcomes Work alongside experienced, collaborative teams Opportunities for …

Added Oct 15, 2026

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Merck (MSD)

Senior Associate, Clinical Research

Gurugram, Haryana, India

Senior Associate, Clinical Research Responsibilities include, but are not limited to: • Trial and site administration: o …

Added Oct 16, 2026

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IQVIA Holdings

Senior Clinical Research Associate

London, United Kingdom

… 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

Clinical Research Associate (CRA)

Remote, Israel

… delays, and execute high-quality, cost-efficient clinical studies. We have an exciting opportunity for Clinical Research Associate (CRA)! Summarized Purpose: Performs and coordinates different aspects of the clinical monitoring and site …

Added Oct 16, 2026

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Becton Dickinson

Clinical Research Associate II

USA AZ - Tempe Headquarters +2 locations

Remote
Full time
Regular

… in, support and/or lead study-specific meetings including, but not limited to study team meetings, Clinical Research Associate team meetings, and vendor meetings. Support Clinical Project Management with other administrative tasks, as …

Added Oct 27, 2026

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IQVIA Holdings

Experienced Clinical Research Associate

Reading, United Kingdom +1 location

Added Oct 15, 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 yourself and your …

Added Oct 27, 2026

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Becton Dickinson

Sr. Clinical Research Associate

USA MD - Sparks - 7 Loveton Circle +36 locations

Remote
Full time
Regular

Pay posted by employer$95,900–$153,400 USD

Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations professional responsible for managing site monitoring and …

Added Oct 31, 2026

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IQVIA Holdings

Senior Clinical Research Associate

Reading, United Kingdom

Added Oct 15, 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 yourself and your …

Added Oct 25, 2026

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IQVIA Holdings

Clinical Research Associate, Early Clinical Development

Carlsbad, California, United States +6 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

FSP Clinical Research Associate II/Senior Clinical Research Associate - Czechia

Remote, Czechia

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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IQVIA Holdings

Senior / Clinical Research Associate

Kuala Lumpur, Malaysia

… 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

Sydney North, New South Wales, Australia +1 location

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate II

Auckland, New Zealand

Step into a dynamic role where you’ll drive innovation and excellence in clinical research. As a key player in our team, you’ll ensure that study sites are not just compliant but thriving, …

Added Oct 15, 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

Amsterdam, The Netherlands

… data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Clinical FSP Business IQVIA clinical FSP business is unique. Our teams are dedicated to a single sponsor partner, …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate (Canada)

Kirkland, Canada

Pay posted by employer$72,100–$152,500

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate I/Clinical Research Associate II - Central Poland

Remote, Poland

Join Us as a Clinical Research Associate I – 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

FSP Clinical Research Associate I/Clinical Research Associate II - Central Poland

Remote, Poland

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REQUIREMENTS · employer excerpt

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical…
Monitoring experience with Oncology
Valid driver's license where applicable.

About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate I – 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.

DESCRIPTION

As part of our global team, you'll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. As a Clinical Research Associate I, 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.
Participates in investigator meetings as necessary. May help to identify 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. Performs 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.
Provides trial status tracking and progress update reports to the team as required. Ensures study systems are complete, accurate and updated per agreed study conventions (e.g. Clinical Trial Management System).
Facilitates effective communication between investigative sites, the client company and internal project teams through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains and completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Contributes to other project work and initiatives for process improvement, as required.

REQUIREMENTS

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.
Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered.
Monitoring experience with Oncology
Valid driver's license 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:

Basic medical/therapeutic area knowledge and understanding of medical terminology
Ability to attain and maintain a working knowledge of ICH GCPs and applicable regulations and procedural documents
Good oral and written communication skills, with the ability to communicate effectively with medical personnel
Good interpersonal skills
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues
Good organizational and time management skills
Ability to remain flexibile and adaptable in a wide range of scenarios
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 manage Risk Based Monitoring concepts and processes
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English and Polish language and grammar skills

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.

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