Munich, Bavaria, Germany · Hybrid
Are you detail-oriented and passionate about supporting clinical research operations? Join our team in Munich as a Project Coordinator (Clinical or Budget&Finance focus), where you’ll play a key role in enabling regulato…
Skills: Regulatory Submissions, Financial Tracking, Investigator Contracts, Document Management, Microsoft Office
Ciudad de México, Mexico · Remote OK
Job Overview: The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment, Pro…
Skills: Project Coordination, Clinical Project Management, Budget Tracking, Risk Management, Vendor Management
Manila, Metro Manila, Philippines · Hybrid
This job post is intended to pool candidates for future job openings within Fortrea's Medical Reviews team. Job Overview: Fortrean Safety Nurses provide medical safety expertise, directly and indirectly, to sponsors of d…
Skills: Pharmacovigilance, Medical Review, Case Assessment, Adverse Event Coding, Narrative Review
Tokyo, Japan · Hybrid
Job Overview: Role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement. Summary of Responsibilities: Acc…
Skills: Grant Payment Management, Transactional Accounting, Clinical Trial Payments, Budget Templating, Financial Reconciliation
Seoul, South Korea · Hybrid
This Senior/Executive Director level role will drive the success of project delivery across South Korea. As an individual contributor this role indirectly oversees a team focused on enhancing project management capabilit…
Skills: Project Management, Leadership, Communication, Strategic Planning, Collaboration
Munich, Bavaria, Germany · Hybrid
Are you detail-oriented and passionate about supporting clinical research operations? If so, join our team in Munich as a Project Coordinator (Budget & Finance focus), where you’ll play a key role in enabling financial w…
Skills: Financial Tracking, Investigator Contracts, Clinical Research Operations, Microsoft Excel, Microsoft Outlook
Leeds, England, United Kingdom · On-site
Fortrea's Clinical Research Unit in Leeds is where life-saving medicines begin their journey. 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 …
Skills: Sample Processing, Laboratory Techniques, Data Documentation, Inventory Management, Hazardous Materials Handling
Leeds, England, United Kingdom · On-site
Fortrea's Clinical Research Unit in Leeds is where life-saving medicines begin their journey. 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 …
Skills: Sample Processing, Laboratory Techniques, Data Documentation, Inventory Management, Hazardous Materials Handling
Budapest, Central Hungary, Hungary · On-site
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, motiva…
Skills: Clinical Trial Setup, Regulatory Submissions, Data Monitoring, Patient Recruitment, Site Management
Durham, California, United States · Remote OK
$185k–$205k/yr
Job Overview: This role sits at the center of Fortrea’s most important client relationships—partnering closely with the Global VP of Sales & Client Services, Business Unit Presidents, Scientific Leadership, and operation…
Skills: Strategic Account Management, Commercial Negotiation, Revenue Growth, Client Retention, Financial Acumen
Dallas, Texas, United States · Remote OK
$160k–$180k/yr
Job Overview: In this role, you’ll drive revenue growth across strategic and complex accounts through proactive outreach, smart networking, and sharp commercial execution. You’ll be the person who connects the dots—culti…
Skills: Business Development, Account Planning, Pipeline Management, Client Relationship Management, Negotiation
Bengaluru, Karnataka, India · Hybrid
Job Overview: Assist with the overall safety system implementation, support, configuration, and migration related activities. Responsible for providing this service to clients either as a support function to the client p…
Skills: Safety Systems Configuration, Data Migration, User Acceptance Testing, Drug Safety Systems, SQL
Warsaw, Masovian Voivodeship, Poland · Remote Solely
Location: Poland (Home-Based) At Fortrea, we are advancing clinical trials through innovative, risk-based approaches and data-driven oversight. We are looking for an experienced Manager, Centralized & Risk-Based Monitori…
Skills: Risk-Based Quality Management, Centralized Monitoring, Risk-Based Monitoring, ICH-GCP, Stakeholder Management
Ciudad de México, Mexico · On-site
Job Overview: Perform and coordinate a variety of tasks to support the company, as part of the leadership of the office service team. Summary of Responsibilities: Order office supplies for firm; perform associated admini…
Skills: Office Management, Administrative Support, Vendor Management, Inventory Management, Records Management
Ciudad de México, Mexico · Hybrid
Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential docum…
Skills: Regulatory Submissions, Site Startup, ICH/GCP Compliance, Document Management, Clinical Trial Process
Madison, Wisconsin, United States · On-site
Come expand and grow your potential leadership and skills at Fortrea as an (onsite) Physician Assistant (PA) based in our Phase I Madison, Wisconsin location supporting clinical trials. The Physician Assistant reports to…
Skills: Physical Examinations, Medical History Taking, Clinical Trial Support, Regulatory Compliance, Patient Assessment
Taipei, Taiwan · 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 Compliance, Document Management, IRB/EC Liaison
Chengdu, Sichuan, 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: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, eCRF Review
Tokyo, Japan · Hybrid
Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential docum…
Skills: Regulatory Submissions, Site Startup, ICH/GCP Compliance, Document Management, Clinical Trial Process
San José, Costa Rica · Remote OK
Clinical Data Specialist – Coordinator 📍 Location: Costa Rica (candidates must be based in Costa Rica) 🧬 Department: Clinical Data Management Advance clinical research through data precision We are looking for a detail…
Skills: Clinical Data Management, Data Quality Checks, ICH-GCP, CDISC, SDTM
Munich, Bavaria, Germany • Hybrid
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Coordinate administrative tasks related to regulatory submissions, financial tracking, and the creation of investigator contracts. Maintain study documentation and liaise with internal teams to ensure data accuracy and timeline adherence.
Requires at least one year of professional experience, preferably in clinical research with a financial or regulatory administrative background. Proficiency in Microsoft Office and fluency in both German and English are essential.
Are you detail-oriented and passionate about supporting clinical research operations? Join our team in Munich as a Project Coordinator (Clinical or Budget&Finance focus), where you’ll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor-dedicated, office-based position offering meaningful exposure to global clinical development.
This role is for upcoming future opportunities that may arise at Fortrea
Key Responsibilities
You will:
If you’re ready to contribute to impactful clinical research through precise coordination and support, we encourage you to apply. We welcome applicants from diverse backgrounds and experiences
#LI-GQ1 #LI-Hybrid
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
