Company · 1,323 open roles

Careers at Fortrea

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Bangalore106Durham98Beijing75São Paulo70Shanghai69Maidenhead62Leeds55Warsaw55

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1,323 positions at Fortrea

CRA II

Fortrea·São Paulo

OnsiteFull-time167d 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

CRA II

Fortrea·São Paulo

OnsiteFull-time167d 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 Research Associate II - Sydney, Melbourne or Adelaide

Fortrea·Melbourne

OnsiteFull-time11d ago

We’re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare. As a CRA2, you will play a key ro…

Medical Writer - Narratives

Fortrea·Bangalore

OnsiteFull-time12d ago

Job Overview: Responsible for preparation and review of clinical documents such as patient safety narratives and clinical study report (CSR) appendices. Responsible for preparing lower complexity documents such as synoptic or abbreviated CSRs under guidance of more senior staff. …

HRSD Specialist I - Operations

Fortrea·Bangalore

OnsiteFull-time12d ago

Job Overview: Service Delivery, People Services Center contact, receives inquiries on service central and provide employee support. Performs workload fulfillment for Service Delivery activities (e.g., HR invoices, offer administration, and employee services) and enters informatio…

Clinical Trial Coordinator (Finance / Supplies)

Fortrea·São Paulo

OnsiteFull-time12d ago

Job Overview The Clinical Trial Coordinator (CTC) serves as a key liaison between investigative sites, sponsors, vendors, and internal study teams, supporting financial and operational activities throughout the clinical trial lifecycle. This role is responsible for coordinating s…

Project Manager Drug Safety

Fortrea·São Paulo

OnsiteFull-time12d ago

Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. …

CRA I/CRA II

Fortrea·Warsaw

OnsiteFull-time12d ago

At Fortrea, your career is more than just a job – it's a journey of innovation, impact, and purpose. Every day, you’ll help advance life-saving therapies and transform the lives of patients around the globe. Together, exceptional is possible. We are currently proactively engagin…

Site Regulatory & Contract Manager - FSP Model - Madrid

Fortrea·Madrid

OnsiteFull-time12d ago

The Site Regulatory & Contract Manager is responsible for leading and overseeing country-level study start-up activities, ensuring clinical trials are initiated on time, within budget, and in compliance with applicable regulations and quality standards. Key Responsibilities • L…

FSP Clinical Research Associate 2 - East Coast - Oncology

Fortrea·Durham

OnsiteFull-time12d ago

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. Seeking candidates on the East Coast with oncology experience. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement t…

FSP Clinical Research Associate 2 - Southeast - Non Oncology

Fortrea·Durham

OnsiteFull-time12d ago

Our FSP team is currently seeking Oncology CRA 2s in Southeast Region! 8-10 days on site per month being a mix of onsite and remote. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical …

CRA I/CRA II

Fortrea·Warsaw

OnsiteFull-time12d ago

At Fortrea, your career is more than just a job – it's a journey of innovation, impact, and purpose. Every day, you’ll help advance life-saving therapies and transform the lives of patients around the globe. Together, exceptional is possible. We are currently proactively engagin…

clinical monitoringich gcp guidelinessite managementsource document verification+11

FSP Clinical Research Associate 2 - Southeast - Non Oncology

Fortrea·Durham

OnsiteFull-time12d ago

Our FSP team is currently seeking Oncology CRA 2s in Southeast Region! 8-10 days on site per month being a mix of onsite and remote. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical …

clinical monitoringsite managementcase report form reviewadverse event reporting+11

FSP CRA I(Shanghai)

Fortrea·Shanghai

OnsiteFull-time12d 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 I (Beijing)

Fortrea·Beijing

OnsiteFull-time12d 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 Trial Coordinator (Finance / Supplies)

Fortrea·São Paulo

OnsiteFull-time12d ago

Job Overview The Clinical Trial Coordinator (CTC) serves as a key liaison between investigative sites, sponsors, vendors, and internal study teams, supporting financial and operational activities throughout the clinical trial lifecycle. This role is responsible for coordinating s…

clinical trial coordinationfinancial managementbudget trackinginvoice management+11

Senior Clinical Data Manager- Oncology- Remote, Canada

Fortrea·Toronto

RemoteFull-time12d ago

Job Overview: • Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from…

clinical data managementoncologygcp complianceproject management+11

HRSD Specialist I - Operations

Fortrea·Bangalore

OnsiteFull-time12d ago

Job Overview: Service Delivery, People Services Center contact, receives inquiries on service central and provide employee support. Performs workload fulfillment for Service Delivery activities (e.g., HR invoices, offer administration, and employee services) and enters informatio…

hr administrationcustomer servicehrmsworkday+11

Site Regulatory & Contract Manager - FSP Model - Madrid

Fortrea·Madrid

OnsiteFull-time12d ago

The Site Regulatory & Contract Manager is responsible for leading and overseeing country-level study start-up activities, ensuring clinical trials are initiated on time, within budget, and in compliance with applicable regulations and quality standards. Key Responsibilities • L…

regulatory submissionsstudy start-upcontract negotiationproject management+11

Project Manager Drug Safety

Fortrea·São Paulo

OnsiteFull-time12d ago

Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. …

adverse event reportingpharmacovigilancemeddra codingfortrea+11

Medical Writer - Narratives

Fortrea·Bangalore

OnsiteFull-time42d ago

Job Overview: Responsible for preparation and review of clinical documents such as patient safety narratives and clinical study report (CSR) appendices. Responsible for preparing lower complexity documents such as synoptic or abbreviated CSRs under guidance of more senior staff. …

patient safety narrative preparationclinical study protocol preparationclinical study report preparationenglish fluency+11

FSO CRA (Tianjin / Shenyang / Changchun / Zhengzhou / Shijiazhuang / Jinan / Harbin / Xi'an)

Fortrea·Beijing

OnsiteFull-time126d 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

FSO CRA (Tianjin / Shenyang / Changchun / Zhengzhou / Shijiazhuang / Jinan / Harbin / Xi'an)

Fortrea·Beijing

OnsiteFull-time126d 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…

Document Specialist II (seeking immediate joiners or with notice period less than 30 days)

Fortrea·Bangalore

OnsiteFull-time13d ago

Job Overview: Responsible for general maintenance and any required archival of documents produced by the CPS Project Management (PM) Team. Organizing, gathering, scanning, and filing of all applicable documents into appropriate electronic and/or paper copy locations, including t…

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What Fortrea hires for

Most-requested skills across active job descriptions.

site managementadverse event reportingclinical monitoringregulatory complianceprotocol adherencetraining deliverystakeholder managementich gcp guidelinesecrf reviewclinical trial management systemssite initiationquality control