fortrea

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 for clinical trials according to Fortrea’s Standard...

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 for clinical trials according to Fortrea’s Standard...

Fortrea is seeking a Lead CRA based in Belgium to manage site monitoring activities for clinical studies in line with ICH GCP, SOPs and sponsor requirements. You will ensure subject protection, data integrity, regulatory document completeness, and audit readiness across sites.The role involves 60% travel to study sites, coordinating with the study team,...

Fortrea in Belgium is seeking a senior FSP sales executive to act as the overall FSP customer expert and strategic business partner. You will drive new opportunities and expand relationships with biotech and large pharma customers, working with BD, Proposal Team, and Strategic Pricing to defend and win RFPs.You will manage the pipeline in SFDC, develop...

Join Fortrea as a Clinical Research Associate and play a key role in advancing impactful clinical research. In this position, you will support the execution of clinical studies that contribute to improving global patient health and driving innovation in life sciences. Key Responsibilities - You will conduct all aspects of study site monitoring, including...

Job Overview Serve as overall FSP customer expert and strategic business partner. Work closely with sales, responsible for developing and expanding new FSP business opportunities with customers. Provide consultative FSP support to potential and existing clients. Establish, grow, and help BD maintain long-term and profitable relationships. Work closely with...

As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan...

A leading global pharmaceutical firm seeks a Senior Statistical Programmer dedicated to delivering complex clinical trials. This role involves developing and validating SAS programs for data analysis. Responsibilities include reviewing study analysis plans, creating datasets, and improving programming efficiency. Applicants should have a relevant degree and...

As a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex projects for a renowned, innovative and global top pharmaceutical company.You will be involved in liaising with the entire study team as needed, including Clinical, Medical Writing, Safety and Biometrics. It...

A leading pharmaceutical firm is seeking a Principal Statistical Programmer to play a crucial role in the delivery of innovative projects. You will oversee programming activities and collaborate with various departments while mentoring less-experienced team members. The ideal candidate has over 5 years' experience in statistical programming within clinical...