Durham, California, United States · Remote OK
$28/hr–$30/hr
Our Phase I team is currently seeking Project Coordinator I to join their growing group! All candidates must reside in the United States. As a leading global contract research organization (CRO) with a passion for scient…
Skills: Clinical research, Project management, Study coordination, GCP, ICH guidelines
Maidenhead, England, United Kingdom · On-site
Are you looking to grow your career in clinical research? Fortrea is hiring an experienced CRA to join our dynamic FSP team. We have opportunities across the UK, with a particular focus on the South West, offering an exc…
Skills: Clinical research, Site monitoring, Regulatory compliance, GCP guidelines, Patient safety
County Laois, The Municipal District of Graiguecullen — Portarlington, Ireland · Remote Solely
What if your project leadership skills helped new medicines take their first step in human clinical trials? Fortrea is one of the world´s largest and longest-established early-phase clinical research organizations. From …
Skills: Clinical Project Management, Clinical Pharmacology, Phase 1 Trials, Phase 1b Trials, Budget Management
Bucharest, Romania · On-site
The Clinical Research Manager (CRM) leads the execution and oversight of clinical trial activities within an assigned country, ensuring compliance with ICH-GCP, local regulations, and company quality standards. Acting as…
Skills: Clinical research, ICH-GCP, Regulatory compliance, Stakeholder management, Clinical trial management
San José, Costa Rica · Remote Solely
Senior Coding Specialist 📍 Costa Rica ✅ Candidates must be based in Costa Rica Are you passionate about medical coding quality and clinical data integrity? We’re looking for a Senior Coding Specialist based in Costa Ric…
Skills: Medical coding, Clinical data integrity, MedDRA, WHO Drug Dictionary, Clinical trial data
Madrid, Community of Madrid, Spain · Remote OK
Job Overview: At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinating site start-up activities, managin…
Skills: Clinical research, Regulatory submissions, Site activation, ICH/GCP guidelines, Document management
Durham, California, United States · Hybrid
Job Overview: Global HR Business Partner and primary HR advisor to senior functional leaders and/or direct reports to C-suite executives supporting complex global functions (IT, Finance and other groups) and organization…
Skills: Human Resources, Strategic Partnership, Organizational Effectiveness, Change Management, Talent Management
Durham, California, United States · On-site
The executives we hire today will define our strategy, shape our culture, drive innovation, and influence outcomes for thousands of employees, customers, and patients around the world.We're seeking an accomplished Execut…
Skills: Executive Search, Talent Acquisition, Stakeholder Management, Executive Compensation, Leadership Assessment
Budapest, Central Hungary, Hungary · On-site
At Fortrea, we believe in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them. …
Skills: Clinical operations, Project management, Study start-up, Site activation, Data forecasting
Hangzhou City, Zhejiang, China · Remote OK
Job Overview: The Senior Process Associate, China Clinical Trial Management Office (CCTMO) provides country support to the country head of Clinical Trial Operations, to identify trends in process performance and formulat…
Skills: Clinical Trial Management, Process Improvement, Project Management, Quality Assurance, CAPA Management
Herzliya, Tel-Aviv District, Israel · Hybrid
oin Our Team and Drive Clinical Research Success! At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinati…
Skills: Clinical research, Regulatory submissions, Site activation, ICH/GCP guidelines, Document management
Kyiv, Ukraine · Remote Solely
Summary of Responsibilities: Management of complex projects under the direction of a Project Manager/Director as assigned.Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Stan…
Skills: Clinical Research, ICH-GCP Guidelines, Trip Report Review, Project Management, Process Improvement
Maidenhead, England, United Kingdom · Remote OK
Are you looking to take the next step in your clinical research career? Fortrea is seeking a CRA II to join our growing FSP team. This is a fantastic opportunity for candidates based in Scotland, where you'll work on a v…
Skills: Clinical Site Monitoring, ICH-GCP, Regulatory Compliance, Site Initiation, Closeout Visits
Durham, California, United States · Hybrid
$160k–$170k/yr
The Director, Global Strategic Sourcing – IT is responsible for leading the strategy, design, and development of a world-class strategic sourcing and category management function across Fortrea’s global Information Techn…
Skills: Strategic Sourcing, Category Management, IT Procurement, Software Licensing, SaaS Contracts
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 Clinical Data Monitor, to interact directly with our healt…
Skills: Clinical data monitoring, Data entry, Quality control, Clinical research protocols, Data planning
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. We are currently seeking a Paramedic, to interact directly with our healthy volunteer…
Skills: Venipuncture, Laboratory Processing, ECG Recording, Vital Signs Monitoring, Clinical Research Protocols
Dallas, Texas, United States · On-site
Join one of the world’s largest Clinical Research Organizations and play a key role in advancing new medical treatments. Our Early Phase Unit is seeking a Lab Technician to support healthy volunteer clinical trials and h…
Skills: Laboratory techniques, Specimen collection, Specimen processing, Lab equipment maintenance, Hazardous materials handling
Dallas, Texas, 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: Paramedic, Clinical Research, Patient Safety, Advanced Cardiac Life Support, Airway Management
São Paulo, São Paulo, Brazil · Remote Solely
Job Overview: Our FSO team is seeking an Oncology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory experience…
Skills: Clinical Project Management, Oncology, Clinical Trials, Budget Management, Risk Management
Lima, Lima, Peru · Remote Solely
Job Overview: At times working under the direction of a Project Director, the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and manag…
Skills: Project Management, Clinical Trials, Drug Development, Risk Management, Stakeholder Management
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
The Project Coordinator will support the delivery of Phase I clinical trials by managing study documentation, timelines, and cross-functional communication. They are responsible for maintaining systems like CTMS and eTMF while acting as a primary point of contact for internal teams and external sites.
Candidates must possess a degree in life sciences or equivalent experience along with 2-3 years of clinical research experience. Proficiency in GCP/ICH guidelines and strong organizational and communication skills are required for this role.
Our Phase I team is currently seeking Project Coordinator I to join their growing group! All candidates must reside in the United States.
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 wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Join a team where your work directly supports first-in-human clinical trials and the development of new medicines. As a Project Coordinator, you’ll play a critical role in keeping studies organized, on track, and audit-ready—working alongside experienced project managers and cross-functional teams in a fast-paced, collaborative environment.
Remote based in United States.
What You’ll Do
Coordinate and support delivery of Phase I clinical trials, including external site studies.
Develop and maintain key study documents (project plans, communication plans, risk registers).
Track timelines, milestones, and study progress to ensure successful execution.
Lead and support study meetings, including agendas, minutes, and follow-up actions.
Manage systems such as CTMS and eTMF, ensuring accuracy and compliance.
Act as a key point of contact for internal teams and external sites.
Support feasibility, start-up activities, and vendor coordination.
Contribute to continuous improvement initiatives and help mentor junior team members.
What You Bring
Degree in life sciences or related field (or equivalent experience).
2–3 years of clinical research experience, ideally in early phase studies.
Experience supporting project management or study coordination.
Knowledge of GCP/ICH guidelines and clinical trial processes.
Strong organizational, communication, and problem-solving skills.
Why Join Us
Work on cutting-edge early phase studies at the forefront of drug development
Collaborate with experienced teams in a high-impact, fast-paced environment.
Gain exposure to the full lifecycle of clinical trials.
Grow your career within a global clinical research organization.
Be part of the team that helps bring new therapies to patients—starting from their very first step into clinical trials.
Note: This role does not provide sponsorship.
Work Environment:
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international.
Physical Requirements:
Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Regular and consistent attendance.
Varied hours may be required.
Target Pay Range: $28-30 USD per hour
#LI - Remote
Applications will be accepted on an ongoing basis.
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
