Clinical Trials Jobs in Maidenhead

The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output including but not limited to: ADaM datasets tables figures and listings output and/or QC of requested output is theThe main focus...

The Associate Director (AD) Biostatistics leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions...

Associate Country Clinical Quality Manager (ACCQM)Location: London UK (Hybrid 2 days per week in the office)About the roleFortrea is seeking an Associate Country Clinical Quality Manager to join our UK client-dedicated team. This role is particularly well suited to experienced SCRAs (ideally 4 year...

Location: UK (Scotland Midlands South East & South West preferred) Contract: 12-month fixed-term (with potential extension based on business needs) Model: Client-dedicated role (FSP)Looking to advance your career in clinical research Fortrea is seeking Clinical Research Associates II to join our FS...

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) tea...

 The Country Clinical Operations Manager is the key leader for Clinical Operations at the country level for both internal & external partners. Accountable for the strategic and operational management for clinical operations and clinical site management activities for the assigned country/ies. Respon...