Paris, Ile-de-France, France · On-site
Job Description At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship — it’s a launchpad for your future. As an Intern, you’ll join a global team where c…
Skills: Clinical Trial Setup, Data Monitoring, Regulatory Submissions, Site Management, Patient Recruitment
Paris, Ile-de-France, France · Hybrid
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, ICH GCP Guidelines, Contract Management, Communication Skills
Athens, Attica, Greece · On-site
We are recruiting for multisponsor team in Greece and are currently seeking to hire a Senior CRA I with a permanent and full-time contract. Our positions offer excellent exposure to a range of disease areas, and a real o…
Skills: Clinical Trial Monitoring, Site Management, Stakeholder Management, Patient Safety, Data Integrity
Durham, California, United States · Remote OK
$115k–$120k/yr
Our Phase I team is seeking an Clinical Project Manager II to join our growing team. This role requires 2+ years of global project management experience, with preferred experience in phase I. Candidates must be based in …
Skills: Clinical Project Management, Phase I Studies, Budget Management, Risk Management, Stakeholder Management
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 Technician to interact directly with our healthy volun…
Skills: Laboratory Sample Processing, Specimen Handling, Laboratory Equipment Operation, Biological Specimen Collection, Clinical Research Protocols
Durham, California, United States · Remote OK
$140k–$150k/yr
Our Phase I team is seeking a Sr. Clinical Project Manager to join our growing team. This role requires 4-5+ years of global project management experience, with mandatory experience in phase I. Candidates must be based i…
Skills: Clinical Project Management, Phase I Trials, Budget Management, Risk Mitigation, Stakeholder Management
Shanghai, Shanghai, China · On-site
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: Site Monitoring, ICH GCP Guidelines, Source Data Verification, Clinical Trial Management, eTMF
Milan, Lombardy, Italy · On-site
$32k–$46k/yr
Job Description 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 act…
Skills: Clinical research, Regulatory submissions, Site activation, ICH/GCP guidelines, Regulatory compliance
Beijing, Beijing, China · Hybrid
This role is for upcoming future opportunities that may arise at Fortrea. Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interv…
Skills: Project Management, Clinical Study Management, Risk Management, Line Management, Stakeholder Management
Budapest, Central Hungary, Hungary · Hybrid
Join 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 coordinat…
Skills: Site Start-Up Coordination, Regulatory Submissions, ICH/GCP Guidelines, Document Management, Informed Consent Form Adaptation
Milan, Lombardy, Italy · Hybrid
$35k–$51k/yr
Job Description 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 Specialis…
Skills: Contract Negotiation, Clinical Research, ICH GCP Guidelines, Communication, Organizational Skills
Leeds, England, United Kingdom · Remote OK
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: Project Management, Clinical Research, Budget Management, Risk Mitigation, Client Relationship Management
Durham, California, United States · Remote OK
Our FSO team is seeking an Oncology Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5+ years of global project management experience, with mandatory experience in oncolog…
Skills: Clinical Project Management, Oncology, Drug Development, Clinical Trial Execution, Risk Management
Hangzhou City, Zhejiang, China · On-site
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
Bengaluru, Karnataka, India
This is a dual role of supporting India labour related compliance and being a member of the talent acquisition team Key Responsibilities: LABOUR GOVERNANCE COMPLIANCE • Stay abreast of changes in labour laws, statutory r…
Zurich, Zurich, Switzerland · Remote OK
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: EU-CTR Submission Management, Site Activation, ICF Management, Quality Control, Process Development
Solna, Stockholm County, Sweden · Remote Solely
Site Budget & Contract Lead (Full-Time, Permanent, Remote) - Sponsor dedicated We are currently seeking an experienced Site Budget & Contract Lead to join our team in a full-time, permanent, remote position. This is an e…
Skills: Site Budgeting, Contract Negotiation, Clinical Trial Agreements, Study Startup, Fair Market Value Guidance
Shanghai, Shanghai, China · 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: Site Monitoring, ICH GCP Guidelines, Clinical Trial Management, Source Data Verification, eCRF Review
Solna, Stockholm County, Sweden · Remote OK
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: Site Activation, Study Start-Up, Clinical Operations, Project Management, ICF Creation
Solna, Stockholm County, Sweden · Remote OK
Join 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 coordinat…
Skills: Site Start-up, Regulatory Submissions, ICH/GCP Guidelines, Document Management, Clinical Research
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Support the setup, execution, and closure of clinical trials in France. Liaise with hospital sites and collaborate with Clinical Research Associates on regulatory submissions and data monitoring.
Candidates must be current BSc Life Sciences students with strong communication and organizational skills. A completed relevant placement year is ideally preferred.
At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship — it’s a launchpad for your future.
As an Intern, you’ll join a global team where curiosity, motivation, and fresh ideas are celebrated. You’ll work on meaningful projects, learn from experienced professionals, and see firsthand how clinical research and healthcare innovation change lives.
We don’t expect you to know it all. What matters most is your potential, your drive to learn, and your willingness to grow. With hands-on experience, mentorship, and structured development, we’ll help you build the skills and confidence to succeed.
Your journey to pioneering tomorrow’s breakthroughs starts here!
Location: Rueil Malmaison
Support clinical trial setup, execution, and closure in France
Liaise with hospital sites and research staff
Assist with regulatory submissions and data monitoring
Collaborate with Clinical Research Associates and Start-Up Specialists
Gain exposure to trial feasibility, patient recruitment, and site management
Professional development workshops and mentorship
Opportunities to present your work to senior leaders
A group philanthropic project
Training to support your scientific and career growth
Strong communication and organizational skills
Team player with initiative
Ideally completed a relevant placement year
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
