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

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Thermo Fisher Scientific

SR CRA (Level II)

Remote, Argentina

Join Us as a SR Clinical Research Associate II – 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

CRA (Level I)

Remote, South Africa

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

Safety Reporting Specialist

Hyderabad, Telangana, India

Join Us as a Associate Safety Reporting Specialist – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, …

Added Oct 29, 2026

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IQVIA Holdings

Program Delivery Manager IP Administration

Durham, North Carolina, United States

Pay posted by employer$68,400–$171,000

… Clinical Supply Integrator, CMC Leader, Study Responsible Physician, Study Responsible Scientist, Global Clinical Research Associate, CTL&D Specialist Other Interfaces: Quality and Compliance Manager/Specialist, R&D/Local Operating …

Added Oct 15, 2026

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IQVIA Holdings

CRA 2, Brazil

São Paulo, Brazil

… 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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McKesson

Source Document Specialist

Nashville, Tennessee, United States

In person
Full time

… It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the …

Added Oct 27, 2026

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Thermo Fisher Scientific

CRA (Level II)

Kyiv, Kyiv City, Ukraine

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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Thermo Fisher Scientific

CRA (Level I) - CRA (Level II)

Madrid, Madrid, Spain +1 location

… sign-on bonus considered for qualified candidates** Locations: Madrid and Barcelona ONLY Join Us as a Clinical Research Associate! – Make an Impact at the Forefront of Innovation We're hiring CRA (Level II) to CRA (Level II) in Madrid …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP CRA (Level II)

Sofia, Sofia-Capital, Bulgaria

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 27, 2026

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Thermo Fisher Scientific

Assistant CRA (ACRA) | Brisbane, Perth

Brisbane, Queensland, Australia

Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation! At Thermo Fisher Scientific, you’ll discover meaningful …

Added Oct 16, 2026

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Thermo Fisher Scientific

Assistant CRA

Remote, United Kingdom

PPD, part of Thermo Fisher Scientific are currently hiring for experienced Assistant Clinical Research Associates across the UK. At Thermo Fisher Scientific, you’ll discover meaningful work that makes …

Added Oct 16, 2026

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Abbott Laboratories

Senior Medical Advisor

Mumbai, Maharashtra, India

… and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. • Contributes to implementation of clinical protocols, …

Added Oct 15, 2026

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Thermo Fisher Scientific

CRA Level II/Senior CRA (Thessaloniki/Athens)

Remote, Greece

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation As part of our global team, you’ll have the …

Added Oct 16, 2026

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IQVIA Holdings

CRA 2, Argentina

Buenos Aires, Argentina

Added Oct 15, 2026

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Thermo Fisher Scientific

Medical Director/Sr Medical Director - Rheumatology

Remote, Argentina

… 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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Thermo Fisher Scientific

Medical Director/Senior Medical Director - Dermatology

Remote, Argentina +5 locations

Added Oct 16, 2026

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Thermo Fisher Scientific

Medical Director/Senior Medical Director - Dermatology

Remote, North Carolina, USA

Added Oct 16, 2026

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Becton Dickinson

Principal Engineer – Applied ML/AI Algorithms R&D for Advanced Patient Monitoring

USA CA - Irvine Laguna Canyon

In person
Full time
Regular

Pay posted by employer$129,600–$207,400 USD

… enable earlier intervention, and drive better outcomes. This team operates at the intersection of research, product, and clinical translation. We partner closely with engineering, clinical, regulatory, and product …

Added Oct 27, 2026

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Thermo Fisher Scientific

Expanded Access Manager / Post-Trial Access Specialist - FSP - UK

Remote, United Kingdom

… CRO industry. • Direct experience in clinical research or managed access, for example as a study manager, Clinical Research Associate (CRA), project manager or in a comparable role. • Working knowledge of compassionate use, early access or …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP CRA I/II Gen Med - Respiratory - HIV - Oncology

Remote, Texas, USA

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

Added Nov 4, 2026

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Thermo Fisher Scientific

SR CRA (Level II)

Remote, Argentina

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a SR Clinical Research Associate II – 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.

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.

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.
• 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 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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