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
Participate and/or contribute to BDM and client calls
Undertake post-award, rescue, and standalone feasibility deliverables in alignment with study and client requirements
Engage with patient advocacy groups and site networks to support study feasibility, recruitment, and successful delivery
Support analysis of collected site data to provide accurate site identification, enrollment modeling and study strategies
Support business development and operational strategy teams and participate in projects to drive innovation and maintain competitive edge
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)
Postgraduate degree preferred
Demonstrates knowledge of ICH-GCP
Advanced computer skills, specifically with MS Word, Excel, PowerPoint, and with web/data-based platforms
Strong IT platform and data analysis skills
Strong presentation abilities
Benefits
Remote work (UK, Spain, Hungary, Poland, Romania, Serbia, Slovakia)
Applicant Tracking System Keywords
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