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Careers at Fortrea

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1,211 positions at Fortrea

Business Development Director II - West Coast

Fortrea·2 Locations

OnsiteFull-time67d ago

We are seeking a results-driven sales professional to manage and grow assigned accounts while delivering against revenue targets. This role focuses on building strong client relationships, developing strategic account plans, and identifying new business opportunities. You will l…

Centralised Clinical Team Lead

Fortrea·Bangalore, Karnataka, India

OnsiteFull Time55d ago

Centralised Clinical Team Lead at Fortrea. Location: Bangalore, Karnataka, India. Role: managing projects, ensuring compliance, mentoring staff Requirements: Lead clinical operations and site monitoring per SOP/ICH‑GCP, review Trip Reports, mentor staff, drive process improvement…

Clinical Research Nurse, Early Phase Clinical Trials - Daytona Beach, FL (On-Site)

Fortrea·Daytona Beach, Florida, United States

OnsiteFull Time89d ago

Clinical Research Nurse, Early Phase Clinical Trials - Daytona Beach, FL (On-Site) at Fortrea. Location: Daytona Beach, Florida, United States. Role: administering compounds, monitoring vitals, documenting events Requirements: Active nursing licensure, associate or BS in nursing,…

Clinical Data Specialist- Costa Rica (Home Based)

Fortrea·San Jose

OnsiteFull-time67d ago

🚀 We’re hiring: Clinical Data Specialist – Clinical Data Management (Costa Rica) 📍 Location: Costa Rica (candidates must be currently based in Costa Rica) Do you enjoy turning complex lab data into clean, reliable clinical insights? Join our Clinical Data Manageme…

clinical data managementlaboratory data managementich/gcp complianceveeva vault+8

Clinical Research Nurse, Early Phase Clinical Trials - Daytona Beach, FL (On-Site)

Fortrea·Daytona Beach

OnsiteFull-time89d ago

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 Clinical Research Nurse, to interact directly with our healthy volunteer participants while learning to read clinical…

clinical researchnursing assessmentcpr/aedinformed consent administration+11

Senior Regulatory Medical Writer

Fortrea·Leeds

OnsiteFull-time67d ago

Sponsor-dedicated. Full time. Remote in the UK, Spain, South Africa, Greece, Portugal or Hungary. We are on a mission to deliver solutions that bring life-changing treatments to patients faster. But we can´t do it alone.   We are seeking an experienced Senior Regulatory Medica…

regulatory medical writingclinical regulatory documentsproject leadershipstakeholder management+11

Site Navigator I

Fortrea·Buenos Aires

OnsiteFull-time67d ago

Job Overview: 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 sites,…

ich/gcp compliancesite activationclinical researchra regulations+11

Centralised Clinical Team Lead

Fortrea·Bangalore

OnsiteFull-time67d ago

Summary of Responsibilities: • Management of complex projects under the direction of a Project Manager/Director as assigned. • Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP), ICH Guidelines and GC…

ich gcptrip report reviewclinical researchsop compliance+11

(Principle/Senior) Biostatistician, RWE

Fortrea·Shanghai

OnsiteFull-time67d ago

Summary of Responsibilities: • Perform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetings. • Perform project management activities for identified projects including resource planning, timelines, and mil…

sasstatistical analysisstatistical analysis plansnon-parametric analysis+11

Site Navigator I (Site Activation/IHCRA)

Fortrea·Sydney

OnsiteFull-time67d ago

Job Overview: 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 sites,…

ich/gcp compliancesite activationclinical researchra regulations+11

Centralised Clinical Team Lead

Fortrea·Bangalore

OnsiteFull-time67d ago

Summary of Responsibilities: • Management of complex projects under the direction of a Project Manager/Director as assigned. • Ensure site monitoring responsibility for clinical studies are conducted according to Fortrea Standard Operating Procedures (SOP), ICH Guidelines and GC…

Associate Clinical Data Manager

Fortrea·San Jose

OnsiteFull-time67d ago

Fortrea is expanding its Clinical Data Management team and we're looking for an Associate Clinical Data Manager to join our FSP model. This is a unique opportunity to be part of a growing footprint in the region and contribute to global clinical trials from the start-up phase. J…

Associate Clinical Data Manager

Fortrea·San Jose

OnsiteFull-time67d ago

Fortrea is expanding its Clinical Data Management team and we're looking for an Associate Clinical Data Manager to join our FSP model. This is a unique opportunity to be part of a growing footprint in the region and contribute to global clinical trials from the start-up phase. J…

electronic data captureclinical data managementgcpich guidelines+11

Clinical & Ancillary Supplies Services

Fortrea·Bogotà

OnsiteFull-time90d ago

Job Overview: The Clinical and Ancillary Supplies Services (CASS) Specialist I: Support the delivery of the Clinical and Ancillary supplies component of assigned studies within a country or 1 region. Act as contact with study team during clinical and ancillary start-up activitie…

clinical supply managementancillary supply managementimportation logisticslabel review+11

Clinical & Ancillary Supplies Services

Fortrea·Bogotà

OnsiteFull-time90d ago

Job Overview: The Clinical and Ancillary Supplies Services (CASS) Specialist I: Support the delivery of the Clinical and Ancillary supplies component of assigned studies within a country or 1 region. Act as contact with study team during clinical and ancillary start-up activitie…

FSP CRA II (Nanjing)

Fortrea·Nanjing

OnsiteFull-time93d 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 compliancesite managementsite initiation+11

FSP CRA II (Nanjing)

Fortrea·Nanjing

OnsiteFull-time67d 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 II (Guangzhou)

Fortrea·Guangzhou

OnsiteFull-time67d 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…

Solutions Consultant - Clinical IT Platforms (FIT)

Fortrea·2 Locations

OnsiteFull-time67d ago

The Solutions Consultant, Digital Health and Innovation Senior Director (FIT) is a senior, customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO, FSP, and SaaS clinical…

Solutions Consultant - Clinical IT Platforms (FIT)

Fortrea·Leeds

OnsiteFull-time67d ago

The Solutions Consultant, Digital Health and Innovation Senior Director (FIT) is a senior, customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO, FSP, and SaaS clinical…

clinical trial technologiesregulatory guidelinesdigital health solutionsgcp+11

FSP CRA II (Guangzhou)

Fortrea·Guangzhou

OnsiteFull-time67d 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

FSO CRA I/CRA II(Changsha)

Fortrea·Chengdu

OnsiteFull-time67d 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…

Associate Clinical Data Manager

Fortrea·Bangalore

OnsiteFull-time67d 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 st…

Data Architect

Fortrea·2 Locations

OnsiteFull-time67d ago

Job Overview: Informatics at Fortrea is a high profile, high impact team that focuses on creating innovative data-driven solutions to improve the speed, cost, and quality of drug development. Summary of Responsibilities: • Contribute to architectural vision for Fortrea’s data …

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stakeholder managementclinical researchich/gcp compliancestakeholder communicationdata validationdocument managementproject managementtraining deliveryich guidelinesdata analysisclinical data managementveeva vault