Leeds, England, United Kingdom · On-site
We exist to bring new medicines to life. What if your administrative support expertise could help us accelerate that journey? FORTREA IN LEEDS – WHERE MEDICAL BREAKTHROUGHS BEGIN At Fortrea, our world-class Clinical Rese…
Skills: Administrative Support, Clinical Trial Recruitment, Data Collation, Quality Control, Record Keeping
Durham, California, United States · Hybrid
$100k–$115k/yr
Our FSP team is currently seeking Unblinded CRAs with 1-3 years of monitoring! Candidates must resided within the United States. 8-10 days on site per month being a mix of onsite and remote. Open to West coast, Central a…
Skills: Clinical Monitoring, Site Management, Case Report Forms, SAE Reporting, Registry Management
Durham, California, United States · Remote OK
$115k–$130k/yr
Regulatory Affairs Project Manager, US Remote Based Fortrea is seeing a seasoned Project Manager with experience aligned with primary work in regulatory space. This role is accountable for communicating updates and issue…
Skills: Project Management, Regulatory Affairs, Budget Management, Risk Mitigation, Clinical Development
Seoul, South Korea · Remote OK
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required.…
Skills: Site Management, Regulatory Compliance, ICH/GCP Guidelines, Clinical Study Start-up, Contract Negotiation
Bangkok, Thailand · Hybrid
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including veri…
Skills: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, eCRF Review
Barcelona, Catalonia, Spain · Remote OK
Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicated Europe remote based Medical Director or Senior Medical Director with deep expert…
Skills: Medical Monitoring, Ophthalmology, Clinical Trial Design, Cell and Gene Therapy, Drug Development
Daytona Beach, Florida, United States · On-site
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a …
Skills: Venipuncture, Blood Pressure Monitoring, ECG/Holter Recording, Biological Sample Processing, Clinical Research Protocols
São Paulo, São Paulo, Brazil · Remote OK
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required.…
Skills: Site Management, Regulatory Compliance, ICH/GCP Guidelines, Clinical Study Start-up, Contract Negotiation
Ciudad de México, Mexico · Remote OK
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required.…
Skills: Site Management, Regulatory Compliance, ICH/GCP Guidelines, Clinical Trial Start-up, Contract Negotiation
Oeiras, Portugal · On-site
Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing …
Skills: Pharmacovigilance, Project Management, Adverse Event Reporting, MedDRA Coding, Regulatory Compliance
Madison, Wisconsin, United States · On-site
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Lab Sample Coordinator (On-Call), to interact directly wit…
Skills: Sample Coordination, Clinical Research Protocols, Biohazardous Shipping, Specimen Collection, Laboratory Procedures
Durham, California, United States · Remote OK
$80k–$105k/yr
The Workflow Manager Pharmacovigilance Operations is responsible for overseeing, optimizing, and ensuring the efficient execution of end-to-end case processing and safety workflows. He/she will be expected to comply with…
Skills: Pharmacovigilance, Case Processing, Workflow Management, Resource Utilization, KPI Monitoring
Daytona Beach, Florida, United States · On-site
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating coverage. We are currently seeking a Screening R…
Skills: Data Entry, Reception, Administrative Support, Quality Control, Time Management
São Paulo, São Paulo, Brazil · Remote OK
Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing …
Skills: Pharmacovigilance, Project Management, Adverse Event Reporting, MedDRA Coding, Regulatory Compliance
São Paulo, São Paulo, Brazil · On-site
Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/I…
Skills: Site Start-Up, Regulatory Submissions, ICH GCP Guidelines, IRB/IEC Regulations, Document Collection
São Paulo, São Paulo, Brazil · On-site
Job Overview: Prepares and negotiates and assists in the execution and retention of site agreements, confidentiality agreements, letters of indemnification and other contracts for Sponsors who contract Fortrea to perform…
Skills: Contract Negotiation, Contract Administration, Site Agreements, ICH GCP, Legal Drafting
Durham, California, United States · Remote OK
$45k–$50k/yr
Our FSP team is currently seeking an CTA to join our growing team! Candidates must be within the United States. Job Overview: The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team respo…
Skills: Clinical Trial Administration, TMF Management, GCP Guidelines, ICH Guidelines, Microsoft Office Suite
Durham, California, United States · Remote OK
$125k–$135k/yr
Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2+ years of global project management experience, with experience in cell & gene therapy. Candidates mu…
Skills: Clinical Project Management, Cell & Gene Therapy, Budget Management, Risk Management, Stakeholder Management
Madrid, Community of Madrid, Spain · Remote OK
Join Our Team and Shape the Future of Clinical Research! At Fortrea, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist, you will play…
Skills: Contract Negotiation, Clinical Research, Budget Planning, Fair Market Value Benchmarking, Grant Management Systems
Durham, California, United States · Remote OK
$105k–$120k/yr
The QA Compliance Lead Auditor (GCP Auditor) is a senior‑level role that is US remote based with preference for candidates near Durham, NC location. This position is within Fortrea’s Global Quality Assurance organization…
Skills: GCP Auditing, Regulatory Compliance, Risk-Based Assessment, CAPA Development, Quality Metrics Reporting
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Support the Clinical Operations team by collating health screening data and managing the selection of eligible participants for clinical trials. Act as a central hub for subject information, ensuring accurate documentation and efficient communication between physicians and study managers.
Requires typically 3+ years of administrative experience with strong organizational skills and proficiency in Microsoft Office. Experience in clinical trials, labs, or hospital settings is an advantage but not essential as training is provided.
We exist to bring new medicines to life. What if your administrative support expertise could help us accelerate that journey?
FORTREA IN LEEDS – WHERE MEDICAL BREAKTHROUGHS BEGIN
At Fortrea, our world-class Clinical Research Unit in Leeds sits at the heart of innovation. Just a short 7-minute walk from the train station, this 65,000 ft², 100-bed facility is a cornerstone of our global operations. Dedicated to Early Clinical Research, it’s where life-saving medicines begin their journey.
And this is where you come in because we are expanding and now seeking our new Clinical Trial Participant Recruitment Administrative Coordinator.
You’ll be part of a team that asks one crucial question: will this new medicine be safe? If you enjoy working in a fast-paced environment, speaking with people and contributing to meaningful research while keeping flexibility in your schedule, this could be a great fit.
This role offers the opportunity to gain experience in a clinical research environment, supporting important studies while working flexibly around other commitments.
You will support our Clinical Operations team in their participant recruitment efforts, ensuring the correct eligibility of participants in the right clinical trial. You will prepare and collate the right data to ensure the selection of quality subjects for specific studies; and you will be the focal point for post-screening data queries within the organization and from clients. You will:
As the person acting as a central hub of subjects´ information and for answering questions within Fortrea and from clients, you will:
One of your main goals will be ensuring that our clinic screening capacities are used to its maximum potential, achieving the maximum number of participants for check-in as possible daily. Communication with participants will be the other key goal and you will co-ordinate the subjects callback process.
If you enjoy staying organised, working with detail, and being part of something that genuinely makes a difference, we’d love to hear from you. Apply now and join us in supporting the next generation of medicines.
Learn more about our EEO & Accommodations request here.
Bringing life-changing benefits to patients faster
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
Offices: Research Triangle Park, NC, US
Bringing life-changing benefits to patients faster
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
Offices: Research Triangle Park, NC, US
