Company · 1,095 open roles

Careers at Fortrea

Fortrea has 1,095 active roles on ResuMinder right now. Score your CV instantly and use the ResuMinder extension to apply in seconds — no manual form-filling.

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Bangalore66Shanghai64Beijing63Durham63Leeds53São Paulo49Maidenhead47Warsaw36

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1,095 positions at Fortrea

FSP CRA II (Beijing)

Fortrea·Beijing

OnsiteFull-time1d ago

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 verification of study training records. • Conducts site monit…

clinical site managementich gcp complianceclinical monitoringsite initiation+11

Contract Specialist II

Fortrea·Warsaw

OnsiteFull-time1d ago

Are you an experienced contracts professional looking to take the next step in your clinical research career? Join us as a Contract Specialist II and play a key role in negotiating and executing clinical trial agreements that support the delivery of innovative studies across the …

contract negotiationclinical trial agreementssite agreementsconfidentiality agreements+11

FSP CRA I (Beijing)

Fortrea·Beijing

OnsiteFull-time1d ago

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: • Respons…

site monitoringsite managementregulatory complianceclinical trial management system+8

Clinical Research Associate II - Barcelona

Fortrea·Barcelona

OnsiteFull-time1d ago

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: • Responsible for all a…

site monitoringsite managementich gcp guidelinesregulatory compliance+11

Clinical Research Associate II - Madrid

Fortrea·Madrid

OnsiteFull-time1d ago

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: • Responsible for all a…

site monitoringsite managementich gcp guidelinesregulatory compliance+11

Project Financial Analyst 1

Fortrea·Bangalore

OnsiteFull-time1d ago

Job Overview: Do you have proven experience working as a project/financial analyst within a Contract Research Organization (CRO) or pharmaceutical company providing financial insight on international clinical trials? Do you have a natural ability to communicate with key stakehol…

revenue recognitiongaapfinancial analysismicrosoft excel+11

Budget Specialist I

Fortrea·Sofia

OnsiteFull-time1d ago

Prepares master study budgets and country study budgets. Responsible for following SOPs including but not limited to departmental SOPs, as well as completing study related duties in accordance with the processes set forth in the relevant process document. Summary of Responsibili…

budget creationgrantplanstandard operating proceduresclinical research+7

Senior Clinical Research Associate II - FSP Model - Rome - Florence or Bologna Area

Fortrea·Milan

OnsiteFull-time9d ago

Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II assures th…

clinical monitoringsite managementregulatory compliancecra certification+11

Laboratory Technician

Fortrea·Leeds

OnsiteFull-time16d ago

Job Overview: Performs routine laboratory sample processing Summary of Responsibilities: • Follows the laboratory procedures for specimen handling and processing. • Operates laboratory equipment. • Recognizes deviations from expected results and follows up appropriately. • Proc…

laboratory sample processingphlebotomyspecimen handlinglaboratory equipment operation+9

Principal Biostatistician

Fortrea·Warsaw

OnsiteFull-time20d ago

As a Principal Biostatistician at Fortrea, you will play a key role in the design, analysis, and delivery of complex clinical trials, supporting global programs from study design through to regulatory submissions and beyond. Working within our Full Service team, you will partner …

statistical analysisclinical trial designstatistical analysis plan developmentstatistical methods+6

Senior Architect - MDM

Fortrea·Bangalore

OnsiteFull-time22d ago

Job Overview: The Senior Architect will be responsible for designing, implementing, and maintaining the overall architecture of our IT systems to support the organization's current and future needs. The Senior Architect will have a strong background in IT infrastructure, systems …

enterprise data architecturemaster data managementmetadata managementdata governance+11

Unblinded CRA in Germany or in Austria

Fortrea·Munich

OnsiteFull-time29d ago

Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As an unblinded Clinical Research Associate , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global en…

unblinded monitoringich-gcp guidelinesclinical trial monitoringinvestigational product management+9

Core CRA (Nanjing/Hangzhou/Anhui/Suzhou)

Fortrea·Nanjing

OnsiteFull-time2d ago

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 verification of study training records. • Conducts site monit…

clinical monitoringich gcp guidelinessite managementsource data verification+11

FSP CRA I (Wuhan/Nanchang)

Fortrea·Guangzhou

OnsiteFull-time3d ago

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: • Respons…

site monitoringclinical trial managementregulatory guidelines compliancecase report form review+11

FSP CRA II (Beijing)

Fortrea·Beijing

OnsiteFull-time3d ago

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 verification of study training records. • Conducts site monit…

clinical site managementich gcp complianceclinical monitoringsite initiation+11

Senior Medical Director

Fortrea·Tokyo

OnsiteFull-time3d ago

Job Overview: Provides medical direction for the conduct of early clinical trials. Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise, as well as medical monitoring assigned clinical studies. Summary of Responsibilit…

clinical trial managementdrug developmentmedical monitoringclinical research+11

Site Navigator II

Fortrea·Tokyo

OnsiteFull-time3d ago

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. Serving as the single point of contact for investigative si…

ich/gcp complianceclinical trial site activationra regulationsirb/iec regulations+11

FSP CRA I (Beijing)

Fortrea·Beijing

OnsiteFull-time3d ago

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: • Respons…

site monitoringsite managementregulatory complianceclinical trial management system+8

Senior Site Navigator

Fortrea·Tokyo

OnsiteFull-time3d ago

Job Overview: Senior Site Navigators play 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. Serving as the single point of contact for investigative…

ich/gcp guidelinesra regulationsirb/iec regulationssite activation+11

FSP CRA II (Beijing)

Fortrea·Beijing

OnsiteFull-time3d ago

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 verification of study training records. • Conducts site monit…

clinical site managementich gcp complianceclinical monitoringsite initiation+11

Clinical Research Associate I in Germany or in Austria

Fortrea·Munich

OnsiteFull-time16d ago

Are you ready to take the next step in your clinical research career and transition into a Clinical Research Associate role? We are looking for motivated professionals with experience as a Study Nurse, Study Coordinator, Clinical Trial Assistant (CTA), or In-House CRA who are ea…

clinical trial monitoringich-gcp compliancegerman language proficiencyenglish language proficiency+11

Site Navigator I based in Germany or Austria

Fortrea·Munich

OnsiteFull-time22d ago

Join Fortrea’s mission to transform clinical trials and improve patient outcomes. As a Study Start Up Site Navigator I in Germany or Austria, you’ll support site activation activities and help ensure smooth collaboration between study teams and clinical sites. Key Responsibilit…

site navigationclinical researchgerman languageenglish language+11

Senior Corporate Counsel

Fortrea·Shanghai

OnsiteFull-time3d ago

Job Overview: The Global Corporate Compliance & Privacy Counsel supports the design, implementation, and continuous improvement of Fortrea’s global compliance and privacy programmes. Working within a collaborative, team-based counsel model, the role helps maintain a consistent, r…

legal counsel licensecompliance frameworksdata protection frameworkspipl+11

Clinical Research Associate based in Germany or in Austria

Fortrea·Munich

OnsiteFull-time3d ago

Be the connection between science and solutions. As a Clinical Research Associate, you will take the next step in your clinical research career, supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professiona…

clinical trial monitoringsite initiationich-gcp compliancesource data verification+11

Tech stack signals

What Fortrea hires for

Most-requested skills across active job descriptions.

site managementclinical trial management systemstakeholder managementtraining deliveryregulatory compliancecase report form reviewsite monitoringclinical monitoringsite initiationclinical researchiso 14155project planning
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