Company · 1,323 open roles

Careers at Fortrea

Fortrea has 1,323 active roles on ResuMinder right now. Score your CV instantly and use the ResuMinder extension to apply in seconds — no manual form-filling.

Active roles
1,323

Refreshed continuously

Median salary
—

Across active listings

Top hirers
Hottest cities
Bangalore106Durham98Beijing75São Paulo70Shanghai69Maidenhead62Leeds55Warsaw55

All open roles

1,323 positions at Fortrea

CRA II - SCRA I - Midlands - FSP

Fortrea·Maidenhead

OnsiteFull-time4d ago

Are you looking to grow your career in clinical research? Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK, particularly in the Midlands, offering an exciting chance to work on diverse studies while ensuring compliance with regulat…

site managementregulatory compliancegcp guidelinesstudy monitoring+11

FSP Clinical Research Associate 2 - Central & East Coast - Oncology Preferred

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…

clinical monitoringsite managementcase report form reviewadverse event reporting+11

Site Navigator I (Tianjin)

Fortrea·Beijing

OnsiteFull-time11d 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 guidelinesregulatory complianceclinical researchsite activation+11

Clinical Research Manager

Fortrea·Bucharest

OnsiteFull-time29d ago

The Clinical Research Manager (CRM) leads the execution and oversight of clinical trial activities within an assigned country, ensuring compliance with ICH-GCP, local regulations, and company quality standards. Acting as the primary country-level contact for assigned studies, the…

ich-gcp complianceclinical trial managementregulatory compliancedrug development+11

Site Navigator I

Fortrea·Seoul

OnsiteFull-time7d 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

FSP SSU (Taipei)

Fortrea·Taipei

OnsiteFull-time7d 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 guidelinesra regulationsirb/iec regulationssite activation+11

Project Manager, Study Start-Up (FSP) - Türkiye

Fortrea·Istanbul

OnsiteFull-time7d ago

We are currently expanding our sponsor-dedicated team in Türkiye and are seeking experienced Project Managers, Study Start-Up, to support our continued growth and future opportunities. This hybrid position is based in Istanbul. While this role is for anticipated future opportun…

clinical trial operationsregulatory compliancebudget managementcontract management+11

Clinical Supply Project Manager, Sponsor-Dedicated (FSP), Türkiye

Fortrea·Istanbul

OnsiteFull-time7d ago

We are currently expanding our sponsor-dedicated team in Türkiye and are looking for experienced Clinical Supply Project Managers. This hybrid position is based in Istanbul. While this role is for anticipated future opportunities in Türkiye, we would be delighted to engage wi…

clinical supply chain managementproject managementclinical operationsinventory management+11

Fortrea Internship Program Turkey

Fortrea·Istanbul

OnsiteFull-time7d ago

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, motivation, and fresh ideas are celebrated. You’ll work on meaning…

clinical study managementtherapeutic indication knowledgephase i-iv study managementstart-up associate procedures+7

Site Navigator I

Fortrea·Seoul

OnsiteFull-time7d 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,…

Regulatory Operations Principal Specialist

Fortrea·Mumbai

OnsiteFull-time15d ago

Job Overview: • Perform various project management and regulatory affairs activities for Fortrea clients.Manage team including performance reviews, human resource issues, and assist Senior Management in assigning resources to projects as required. Manage, coordinate and oversee …

dissolution testinggmp complianceanalytical techniqueshplc+11

Regulatory Operations Specialist I

Fortrea·Mumbai

OnsiteFull-time22d ago

Job Overview: • Perform various project management and regulatory affairs activities for Fortrea clients.Manage team including performance reviews, human resource issues, and assist Senior Management in assigning resources to projects as required. Manage, coordinate and oversee …

regulatory affairsquality assurancemethod validationcapa+11

ICF Reviewer II

Fortrea·Bucharest

OnsiteFull-time32d ago

Job Overview: Document Review Specialist II is responsible for reviewing Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP, FDA and other regional guidance. Document Review Specialist II may responsible for reviewing r…

ich-gcp complianceinformed consent form reviewfda regulationsprotocol amendment review+10

TMF Reviewer II

Fortrea·Bangalore

OnsiteFull-time34d ago

Job Overview: Responsible for performing TMF review of electronic Trial Master Files (eTMF), Trial, Country, and Site artifacts for clinical studies in support of sponsors services contracts and internal Fortrea business needs. Summary of Responsibilities: • Position provides p…

tmf reviewelectronic trial master filegcp complianceclinical trial documentation+11

Senior Manager, Process Compliance Review and Analysis

Fortrea·Pune

OnsiteFull-time42d ago

Job Overview: It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health & Safety …

safety writingquality managementcapa managementregulatory compliance+11

Apprentice - IT Product Management (Remote)

Fortrea·Bangalore

RemoteFull-time43d ago

Company Overview: As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patie…

azure devopsagileai projectsmarketing automation+10

Safety System Manager, Argus SME

Fortrea·Pune

OnsiteFull-time42d ago

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 project  groups or as stand- alone business. • Responsib…

arguschange managementhealth & safety compliancesystem integration+11

RWE (Real World Evidence) SAS Programmer, CDISC/SDTM specs

Fortrea·Warsaw

OnsiteFull-time7d ago

Job Overview: The Senior Associate-Real-world Data (RWD) Analyst, in our Fortrea Consulting group, is responsible for supporting our Real-world Evidence (RWE) services through successful delivery of complex analyses of data generated from global prospective and retrospective obse…

sas programmingsdtmr programmingpython programming+11

FSP Clinical Project Coordinator based in Vienna

Fortrea·Vienna

OnsiteFull-time7d ago

Are you detail-oriented and passionate about supporting clinical research operations? Join our team as an FSP Clinical Project Coordinator , where you’ll play a key role in enabling regulatory workflows across clinical studies. This is a sponsor-dedicated, office-based position i…

regulatory submissionsclinical trial coordinationgerman languageenglish language+9

Unblinded CRA based in Austria

Fortrea·Vienna

OnsiteFull-time19d 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+10

Medical call center Associate I

Fortrea·Manila

OnsiteFull-time8d ago

Summary of Responsibilities: • To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. • Receive information, record, and report Adverse Drug Reaction in timelines (according to the regula…

Medical Contact Center Assistant I

Fortrea·Manila

OnsiteFull-time8d ago

Summary of Responsibilities: • To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. • Receive information, record, and report Adverse Drug Reaction in timelines (according to the regula…

FSP CRA II(Changsha/Huizhou/Nanning/Fuzhou/Haikou)

Fortrea·Guangzhou

OnsiteFull-time8d 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/II/S(Nanjing/Hefei)

Fortrea·Nanjing

OnsiteFull-time8d 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…

Tech stack signals

What Fortrea hires for

Most-requested skills across active job descriptions.

regulatory compliancestakeholder managementsite managementcase report form reviewirb/iec regulationsproject managementprocess improvementorganizational skillsclinical researchsite activationcontract negotiationbudget negotiation
Fortrea careers — 1,323 open roles | ResuMinder | ResuMinder