Associate director, feasibility lead - united kingdom, berkshire

details: full-time contract position asap start for minimum 12 month contract remote working in the uk competitive hourly rate of pay global pharma company the role: the feasibility strategic analytics lead (fsal) will be responsible for partnering with clinical study team lead (cstl), participant recruitment (pr), gsso roles, and clinical leads enable the predictable delivery of client's portfolio by providing rapid, accurate and robust assessments of program and protocol feasibility, recruitment enrollment assumptions, and site strategy plans. implementing processes related to country & site intelligence and provide continuity by connecting and documenting changes throughout the lifecycle (from early estimates, early feasibility, detailed assumptions, detailed feasibility, to participant recruitment, study start-up planning and last subject first visit) provides early feasibility (before core protocol elements are available) by providing initial enrollment timelines, potential country footprint, primary intelligence gathering (benchmark studies, competitive landscape, treatment approvals etc), and key enrollment assumptions to inform initial high level op plan assumptions introduces opportunities for protocol optimization by leveraging real world data, investigator insights, patient insights, protocol simulations, and coordinates with relevant functions to incorporate these insights in study assumptions. analyze results of outreach and evidence to build the recommended country and site strategy provide summary site analytics as the volume of sites is progressed through evaluation stages to pre trial assessment (pta) to ultimate site selection. analytics include modeling volume of patients (by site segmentation); ability of site mix to achieve clinical trial diversity goals; competition, site overlap and other key parameters identified as performance drivers by study team operational responsibility for delivering to agreed set of kpis for assigned protocols full job description available on application the candidate: bs / rn / ms & 7 years relevant experience phd / md and 3 years relevant experience knowledge of drug development, a thorough understanding of the processes associated with global country and site feasibility, clinical study start-up and business operations experience in clinical research, including clinical trial conduct, knowledge of gcp and a good understanding of the processes associated with study/project management, monitoring, clinical and regulatory operations experience in operations involving multinational clinical trials is preferred. prior experience in global country and site feasibility preferred only candidates with existing right to work in the uk/eu will be considered to apply: please complete the details below to apply. for further information or a discreet discussion regarding your recruitment requirements, please call alex on or email to view our other vacancies, please visit our website on apex recruitment are a specialist agency providing opportunities within the pharmaceutical, biopharma, biotech and medical device industries recruiting in the areas of medical affairs, drug safety, clinical and quality.

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