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Careers at Fortrea

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Bangalore77Durham75Beijing73Shanghai69São Paulo61Leeds56Maidenhead53Warsaw44

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1,211 positions at Fortrea

FSP CRA II Beijing)

Fortrea·Beijing

OnsiteFull-time46d 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+9

CRAs & Sr. CRAs - Radiopharmaceutical Therapies - Remote US

Fortrea·Remote United States

RemoteFull-time46d ago

We are currently seeking Experienced CRAs with Radiopharmaceutical therapeutic expertise to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. Open to major hub locations across the US. 60-…

clinical monitoringradiopharmaceuticalssite managementdata review+11

Med Data Review Assoc Mgr

Fortrea·Bangalore

OnsiteFull-time46d ago

Job Overview: The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring strategy, such as: Collaborate within a matrix environment, co…

central medical reviewmedical data analysisxcellerate® medical reviewrisk assessment+9

CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada

Fortrea·Toronto

OnsiteFull-time46d ago

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired, seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS …

clinical monitoringsite managementcase report form (crf) reviewdata management+11

Sr. Director Strategic Accounts - Pharma (United States)

Fortrea·Durham

OnsiteFull-time46d ago

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 operational leaders to shape and execute bold global account strategi…

strategic account managementclient relationship managementpharmaceutical salesbusiness development+11

FSP SCRA I (Beijing)

Fortrea·Beijing

OnsiteFull-time46d ago

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, …

clinical site monitoringsite managementregulatory compliancecase report form review+11

FSP CRAI/II (Wuhan)

Fortrea·Shanghai

OnsiteFull-time46d 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

FSP CTC(Shanghai)

Fortrea·Shanghai

OnsiteFull-time46d ago

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/IRB/Third body/Regulatory Authority and any other local appli…

ich guidelinesclinical trial start-upra regulationsirb/iec regulations+10

FSP CTC(Shanghai)

Fortrea·Shanghai

OnsiteFull-time46d ago

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/IRB/Third body/Regulatory Authority and any other local appli…

ich guidelinesclinical trial start-upra regulationsirb/iec regulations+10

FSP CRA I (Beijing)

Fortrea·Beijing

OnsiteFull-time46d 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

FSP CRAII (Beijing)

Fortrea·Beijing

OnsiteFull-time46d 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

Adjudication Coordinator Il

Fortrea·São Paulo

OnsiteFull-time46d ago

Job Overview: Responsible for providing coordination and support of projects operated by the Adjudication Services department, to ensure smooth delivery and achievement of the objective that all adjudication events are processed and submitted for adjudication within the agreed up…

event processingadjudication event tracking systemsdocument processingquality control+10

Med Data Review Assoc Mgr

Fortrea·Bangalore

OnsiteFull-time48d ago

Job Overview: The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring strategy, such as: Collaborate within a matrix environment, co…

Senior CRA II Sponsor dedicated based in Türkiye

Fortrea·Istanbul

OnsiteFull-time52d ago

Join Fortrea as a Senior Clinical Research Associate II in Türkiye within a sponsor-dedicated model, where you will work exclusively with a leading global biopharmaceutical partner. In this role, you will support the delivery of high-quality clinical trials across innovative the…

FSP Clin Trials Admin I (Guangzhou)

Fortrea·Guangzhou

OnsiteFull-time48d ago

Job Overview: The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience, and level of contribution which they …

FSP CTC(Shanghai)

Fortrea·Shanghai

OnsiteFull-time48d ago

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/IRB/Third body/Regulatory Authority and any other local appli…

FSP CTC(Shanghai)

Fortrea·Shanghai

OnsiteFull-time48d ago

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/IRB/Third body/Regulatory Authority and any other local appli…

FSP CRAI/II (Wuhan)

Fortrea·Shanghai

OnsiteFull-time48d 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…

FSP SCRA I (Beijing)

Fortrea·Beijing

OnsiteFull-time52d ago

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, …

FSP CRA I (Beijing)

Fortrea·Beijing

OnsiteFull-time48d 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…

FSP CRA II Beijing)

Fortrea·Beijing

OnsiteFull-time52d 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 Operations Coordinator

Fortrea·Leeds

OnsiteFull-time48d ago

What if you were the person clinical research teams relied on when project plans move into live clinic activity? Fortrea is one of the largest and longest‑established early‑stage clinical research organizations in the world. We operate four Phase I clinical research units glob…

FSP CRAII (Beijing)

Fortrea·Beijing

OnsiteFull-time48d 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…

FSP CRA I (Beijing)

Fortrea·Beijing

OnsiteFull-time48d 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…

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What Fortrea hires for

Most-requested skills across active job descriptions.

stakeholder managementclinical monitoringtraining deliveryclinical trial management systemsite managementregulatory compliancetraining and mentoringclinical site managementich gcp compliancesite initiationdata integrity verificationeclinical systems