Provide pre-award feasibility analysis and input for pre-award RFPs, including competitive analysis, historical recruitment analysis, standards of care, drug analysis, epidemiology analysis, site and country analysis.
Review clinical protocols, study assumptions, client information and study plans for US and global trials.
Present and explain feasibility analysis to BD/Clients, including the process, recommendations, and rationale.
Interface with colleagues, consultants and partners and collaborate with internal and external sources to gather and share feasibility information.
Undertake feasibility site outreach for pre award opportunities.
Undertake post-award, rescue, and standalone feasibility deliverables in alignment with study and client requirements.
Where appropriate, engage with patient advocacy groups and site networks to support study feasibility, recruitment, and successful delivery.
Support the analysis of the collected site data to provide accurate site identification, enrollment modeling and study strategy (ies)
Requirements
Bachelor’s degree in a life sciences discipline
A minimum of 5 years of related experience
Combination of qualifications and equivalent relevant experience may be accepted as an alternative.
Relevant experience in the required activities for the role including feasibility analysis, site identification.
Ability to communicate both verbally and in writing at the English proficiently (Professional level)