Provide pre-award feasibility analysis and input for pre-award RFPs including competitive, historical recruitment, standards of care, drug, epidemiology, 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 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 and participate in 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 and recruitment where appropriate
Support analysis of collected site data to provide accurate site identification, enrollment modeling and study strategy(ies)
Participate in projects to support innovation and maintain scientific and operational competitiveness
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
Postgraduate degree preferred
Relevant experience in feasibility analysis and site identification
Ability to communicate both verbally and in writing in English (Professional level)
Advanced computer skills (MS Word, Excel, PowerPoint)
Experience with web/data-based platforms and data analysis
Knowledge of ICH-GCP
Strong presentation abilities
Willingness to work in a matrix environment and both independently and as part of a team
Benefits
Remote work (UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia)
Reasonable accommodation for applicants with disabilities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.