Jobs at Fortrea (Now Hiring) — 300 open — Page 13

Clinical Team Lead

Tokyo, Japan · Hybrid

Mid level

Job Overview: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and o…

Skills: Clinical Project Management, Site Management, Budget Management, Risk Management, ICH Guidelines

Executive Director, Clinical Platforms and Product Development

Durham, California, United States · Remote OK

Senior+

The Executive Director, Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining, building, and operationalizing Fortrea’s Clinical Platforms ecosystem. This role ser…

Skills: Product Strategy, Clinical Trial Lifecycle, Platform Engineering, Agile Methodology, DevOps

Sr Clin Res Assoc I

Tokyo, Japan · Hybrid

Mid level

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. T…

Skills: Site Monitoring, Site Management, Clinical Research, Regulatory Compliance, Case Report Forms

Contract Assoc II

Tokyo, Japan · Hybrid

Mid level

Job Overview: Prepares and negotiates and assists in the execution and retention of site agreements, confidentiality agreements, letters of indemnification and other contracts for Sponsors who contract Fortrea to perform…

Skills: Contract Negotiation, Contract Administration, Site Agreements, ICH GCP, Legal Drafting

Executive Director, Clinical Platforms & Product Development

Leeds, England, United Kingdom · Remote OK

Senior+

The Executive Director, Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining, building, and operationalizing Fortrea’s Clinical Platforms ecosystem. This role ser…

Skills: Product Strategy, Clinical Trial Lifecycle, Platform Engineering, Agile Methodology, DevOps

Associate II PSS (1 year contract)

Seoul, South Korea · Remote OK

Mid level

Job Overview: Responsible for assisting with overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may include safety data collected from clinical trial…

Skills: Pharmacovigilance, Adverse Event Processing, MedDRA Coding, Patient Narratives, Regulatory Submissions

Research Nurse I

Leeds, England, United Kingdom · On-site

Mid level

Turn Your First Years on the Ward into a New Career Path Have your first 1–2 years on a hospital ward not turned out the way you expected? At Fortrea’s Early Clinical Research Unit in Drapers Yard, Leeds, you can use tha…

Skills: Cannulation, Blood Sampling, ECG, Medicines Administration, Patient Monitoring

Operations Assistant Bank

Leeds, England, United Kingdom · On-site

Entry level

What if the skills you’ve built in hospitality, retail, customer service or other fast‑paced, people‑focused jobs could help bring new medicines to life? Fortrea's Clinical Research Unit in Leeds is where life-saving med…

Skills: Venipuncture, Blood Pressure Monitoring, ECG Recording, Biological Sample Processing, Microsoft Office

Senior Director, Clinical Network

Tokyo, Japan · Hybrid

Senior+

Job Overview: A key operational role within our matrix organization, accountable for the clinical operational activities and performance within an assigned group of countries or delivery team, with responsibilities for c…

Skills: Clinical Operations, Matrix Management, Resource Management, Financial Acumen, Regulatory Compliance

FSP CRAII( Chongqing)

Chengdu, Sichuan, China · Remote OK

Mid level

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 veri…

Skills: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, eCRF Review

Clinical Research Associate II - FSO

Athens, Attica, Greece · Hybrid

Mid level

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 veri…

Skills: Site Monitoring, ICH GCP Guidelines, Source Data Verification, Clinical Trial Management, Regulatory Compliance

FSP CRA II (Kunming)

Chengdu, Sichuan, China · Remote OK

Mid level

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 veri…

Skills: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, eCRF Review

FSP CRA I(Wuhan)

Shanghai, Shanghai, China · On-site

Entry level

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 …

Skills: Site Monitoring, Site Management, Clinical Trial Process, Regulatory Guidelines, ICH GCP

Director of Product Engineering - Clinical Data Management / EDC

Bengaluru, Karnataka, India · Remote OK

Senior+

The Director of Product Engineering will lead the strategy and development of our Data Management Products. This role is pivotal in shaping innovative solutions that meet the evolving needs of our clients in the life sci…

Skills: Product Management, Clinical Data Management, EDC, Agile SAFe, Product Roadmap Development

FSP Clinical Research Assoc. I MEA (Beijing)

Beijing, Beijing, China · Hybrid

Mid level

Job Overview: The Clinical Research Associate I MEA (CRA I MEA) 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 CR…

Skills: Clinical Monitoring, Site Management, ICH Guidelines, GCP, Source Document Review

FSP CTAI (Beijing)

Beijing, Beijing, China · Hybrid

Entry level

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 ref…

Skills: Clinical Trial Administration, TMF Management, Project Tracking, Document Control, Microsoft Office Suite

FSP CRA II(Wuhan)

Shanghai, Shanghai, China · Hybrid

Mid level

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 veri…

Skills: Site Monitoring, ICH GCP Guidelines, Clinical Trial Management, Source Data Verification, eCRF Review

FSP CRA II (Wuhan/Nanchang)

Shanghai, Shanghai, China · Hybrid

Mid level

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 veri…

Skills: Site Monitoring, ICH GCP Guidelines, Source Data Verification, Clinical Trial Management, Regulatory Compliance

Manager, Clinical Data Management

San José, Costa Rica · Hybrid

Senior+

Fortrea is expanding its Clinical Data Management team and we're looking for a Manager, Clinical Data Management (CDM) to join our organization. This is an exciting opportunity to lead and develop high-performing data ma…

Skills: Clinical Data Management, People Management, Resource Planning, Workforce Planning, ICH-GCP Guidelines

FSP CRA II(Guangzhou/Fuzhou/Xiamen/Nanning)

Guangzhou City, Guangdong Province, China · Hybrid

Mid level

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you …

Skills: Clinical Monitoring, ICH GCP Guidelines, Site Management, Source Data Verification, eCRF Review

About Fortrea

Bringing life-changing benefits to patients faster

Industry
Biotechnology Research
Company size
10,001+ employees
Headquarters
Research Triangle Park, NC
LinkedIn followers
253,042

Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com

Offices: Research Triangle Park, NC, US

clinical researchclinical trialsand medical device trialsHealth CareClinical Trials
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