Point your AI agent at freehire and let it find you a job. A CLI and an MCP server over the whole job API — no browser.
The Site Navigator Intern supports site-level activities throughout study start-up and, maintenance and closeout. Under the guidance of experienced team members, the intern assists with feasibility, site outreach, site…
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…
Job Overview: Responsible for the management, administration, and organization of local site operations for a Clinical Pharmacology unit, may take on responsibility for multiple sites. Responsible for the overall…
Job Description We are looking for a Regulatory Submissions Ass Manager II to support global and regional clinical trials through high‑quality regulatory submissions across Europe and beyond. This role plays a critical…
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 Paramedic, to interact directly with our healthy volunteer…
Job Description: Fortrea has an exciting opportunity for a Human Resources Specialist to join the HR Service Delivery Team! The Human Resources Specialist will act as a key contributor within the HR Service Delivery…
Job Overview: The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight, and impact on local regulatory and financial compliance, at a country…
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 & in the Central region, oncology preferred.…
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 in the San Francisco, CA area or West Coast with Oncology. WHAT YOU…
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 in the Las Vegas, NV area with Oncology. WHAT YOU WILL DO You will…
Fortrea is currently recruiting for an FSP Lead Data Manager for a global pharmaceutical project. This position can be based in either Beijing or Shanghai. Key Responsibilities Very strong subject matter expertise in…
Job Overview: The QA Associate Director, APAC ex-India serves as a strategic regional RC&QA solutions partner, providing line management and day-to-day quality leadership across APAC ex-India. The role reports to…
Job Overview: The Intern will support departmental operations and project-based initiatives. This role offers hands-on experience in a corporate environment, contributing to both strategic and administrative functions…
Bedside Data Capture (BDC) Study Designer Joining Fortrea’s Bedside Data Capture (BDC) team offers an exciting opportunity to contribute to the successful delivery of Phase I clinical studies through innovative…
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…
Location: Hybrid (2 days per week in the Central London office) We are seeking a Study Start-Up Project Manager to join our team. In this role, you will work 100% dedicated to a leading global pharmaceutical company,…
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…
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…
Reporting to the Director, Global IT Quality and Compliance (IT Q&C), the Sr. Manager, IT Quality and Compliance is a member of the Global IT Quality and Compliance leadership team and responsible for assisting the…
Job Overview: Reviews trip reports, proactively identifies risks and communicate any trends, outstanding issues, safety concerns to the study team. Responsible for the execution of key Central monitoring activities…
We couldn't check your fit for this role — add a CV to your profile to see it next time.