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

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Thermo Fisher Scientific

Senior Clinical Research Associate I

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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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, North Carolina, USA

CRA (Level II) 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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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

Experienced Clinical Research Associate - CZ Republic

Prague, Czech Republic

… University degree in scientific discipline or health care At least 2 year of experience as a Clinical Research Associate. Very good computer skills including MS Office Excellent command of Czech and English language. CZ Republic …

Added Oct 15, 2026

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Thermo Fisher Scientific

Clinical Research Associate (CRA) - Multiple Levels

Istanbul, Turkey

Clinical Research Associate (CRA) Location: Istanbul, Türkiye Fully Remote At Thermo Fisher Scientific, you’ll discover meaningful work …

Added Oct 16, 2026

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IQVIA Holdings

Clinical Research Associate Trainee Program (Sydney)

North Sydney, New South Wales, Australia

Clinical Research Associate Trainee Program Sydney- Now taking applications for our next intake commencing on the 1st February 2027. …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate Trainee Program (Melbourne)

Melbourne, Australia

Clinical Research Associate Trainee Program (Melbourne) - Now taking applications for our next intake commencing on the 1st February …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate Trainee Program (Adelaide)

Melbourne, Australia

Clinical Research Associate Trainee Program (Adelaide) - Now taking applications for our next intake commencing on the 1st February …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior Clinical Research Associate (Sr CRA)

Remote, Egypt

Join Thermo Fisher Scientific Inc. as a Sr. Clinical Research Associate in our newly created entity in Egypt! This is an outstanding opportunity to contribute to groundbreaking …

Added Oct 20, 2026

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IQVIA Holdings

Clinical Research Associate, Sponsor Dedicated, Oncology

Overland Park, Kansas, United States +3 locations

Pay posted by employer$90,200–$197,500

Site Visits: Conduct selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Recruitment Drive: …

Added Oct 15, 2026

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Thermo Fisher Scientific

Clinical Research Associate (CRA) – Multiple Levels

Remote, Poland

… 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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IQVIA Holdings

Experienced Clinical Research Associate, FSP Belgium

Zaventem, Belgium

… the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate, South West England

Bath, United Kingdom +1 location

… 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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IQVIA Holdings

Experienced Clinical Research Associate FSP Romania

Bucharest, Romania

Added Oct 15, 2026

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IQVIA Holdings

Senior Clinical Research Associate - Sponsor Dedicated

Amsterdam, The Netherlands

… clinical research expertise to drive meaningful outcomes for patients and sponsors around the world. As a Clinical Research Associate, you'll work across innovative studies and therapeutic areas, build your reputation with leading …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate - IQVIA Biotech Poland

Warsaw, Poland

… care or other scientific discipline or educational equivalent 2 years on-site monitoring experience of clinical trials (ideally in CVRM/Oncology) Written and verbal communication skills including good command of Polish …

Added Oct 15, 2026

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Thermo Fisher Scientific

Clinical Research Associate (CRA) - Client-dedicated

Remote, Turkey

Added Oct 16, 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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IQVIA Holdings

Clinical Research Associate 2 - IQVIA Biotech

Madrid, Spain +1 location

I QVIA Biotech is hiring Clinical Research Associate in Spain! IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support …

Added Oct 15, 2026

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Merck (MSD)

Associate. Director, Clinical Research-Immunology Early

CHN - Shanghai - Shanghai (Tower A)

Will conduct early clinical studies in Immunology field. Required Skills: Adaptability, Adaptability, Cell Physiology, Clinical …

Added Oct 16, 2026

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Thermo Fisher Scientific

Senior Clinical Research Associate I

Auckland, New Zealand +1 more

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Experience · employer excerpt

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4+ years as a clinical research monitor).
Monitoring experience in phase-I healthy volunteers studies is essential.

About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find 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 resident in New Zealand, located within proximity of a well-connected air travel hub, ideally in Auckland or Christchurch.

About the Role:

Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors. Acts as a site processes specialist, ensuring 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. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to 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.
Maintains 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.
May participate 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 and remote 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

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Valid New Zealand driver's license is required and ability to drive.

Experience

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4+ years as a clinical research monitor).
Monitoring experience in phase-I healthy volunteers studies is essential.

Knowledge, Skills, 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
Good English language and grammar skills
Good presentation skills

Other Important Information

This position will also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. Actual compensation will be confirmed in writing at the time of offer. We offer a comprehensive Total Rewards package that our NZ colleagues can count on.

Benefits

Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer.

Health & Wellbeing: Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues.
Flexibility: Balance your work and personal life with flexible arrangements.
Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.
Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you.
Learning & Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 125,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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