fortrea

Job Overview: Responsibility for delivering EDC design and specifications within the scope of assigned projects to achieve project integrity and the delivery of on-time, quality data. Document and maintain contents of the standards library as required. Lead eCRF Design within the scope of assigned p

Senior Clinical Scientist, FSP – Immunology – Remote US or Canada ***Position leads Phase 1-3 Clinical Trials and oversees medical monitoring. This is not a laboratory/research scientist role.*** In this role, the selected candidate will lead/support studies; be accountable for the clinical/scientif

Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with sponsors, legal teams, clinical operations, and study teams to facilitate timely contract execution.

We are seeking a CRA I or CRA II to support a routine post-market surveillance study within a dedicated FSP model. Key responsibilities include: Monitoring investigator sites across the North of England. Building strong relationships with investigators and site teams. Ensuring patient safety, data q

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 CRM drives study pe

Senior Clinical Data Manager (remote or hybrid) – Full Service Do you have experience leading data management activities across late phase studies? Are you looking for a new challenge in an environment where you be closely supported by your Manager, peers and Senior Leaders in your team? Join our gr

Job Overview: Senior 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, this role en

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 (On-Call), to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enj

Job Description As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. As a Clinical Research Technician II you will perform practical / administrative activities of clinical trials in Clinical Pharmacology in line with

Job Overview: The Procurement and Supply Chain Manager is an individual contributor responsible for leading strategic sourcing, supplier management, inventory management, and supply chain operations supporting Fortrea’s Clinical Pharmacology Services (CPS) business, including laboratory and Clinical

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 monitoring responsibilities fo

FSP Clinical Scientist III / Medical Science Liaison – US Remote based Fortrea is hiring a Medical Science Liaison (MSL) – FSP to provide ongoing in-depth analysis and scientific input into development and execution of protocols and clinical development plans by working with the medical/scientific/r

Clinical Research Licensed Practical Nurse (LPN) / Paramedic - Early Phase Clinical Trials Location: Daytona Beach, FL Schedule Options: Option 1: Rotating Shift 10-hour shifts Rotating weekends to include a 12-hour shift Option 2: Mid Shift 10-hour shifts Start time between 11am and 1pm Rotating we

Clinical Research Licensed Practical Nurse (LPN) / Paramedic - Early Phase Clinical Trials (Multiple Shifts Available) Location: Daytona Beach, FL Schedule Options: Option 1: Rotating Shift 10-hour shifts Rotating weekends to include a 12-hour shift Option 2: Mid Shift 10-hour shifts Start time betw

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 at Work Act 1974, the

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.• Responsible for providing all clie

Have you ever wanted to see a clinical trial happen in real time? This is not monitoring from a distance. At Fortrea Clinical Pharmacology Services in Leeds, CRAs are on site, in the flow of the study, when it matters most. You see dosing days . You walk the clinic floor. You review data as it is ge

Join Our Team and Drive Clinical Research Success! At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulat

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. The Senior CRA I assure the implementation of project plans, as assigned. Functio

Job Overview: Document Review Specialist I 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 I may responsible for reviewing revised protocols and c