Support pre-award feasibility projects, providing analysis and input for RFPs including competitive, historical recruitment, standards of care, drug, epidemiology, site and country analyses
Review clinical protocols, study assumptions, client information and study plans for US and global trials
Present and explain feasibility analysis to BD/Clients including process, recommendations and rationale
Interface with colleagues, consultants and partners; undertake feasibility site outreach and participate in BDM and client calls
Provide support to 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 and recruitment
Support analysis of collected site data to provide site identification, enrollment modeling and study strategies
Support stand-alone feasibility projects and provide feasibility support for newly awarded and ongoing projects
Participate in projects to drive innovation and maintain competitive scientific advantage
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
Applicant Tracking System Keywords
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