Senior Global Feasibility Lead – Sponsor Dedicated

This is a fully remote position, open to applicants in United Kingdom, +3 more countries.

📋 Description

• Work autonomously with minimal supervision on RFP and standalone paid feasibility objectives across all therapeutic indications.

• Evaluate data and analysis requirements while proposing methodologies for RFPs and individual paid feasibility assessments.

• Oversee multiple projects of varying complexity simultaneously across different therapeutic areas.

• Identify solutions for non-standard requests and leverage knowledge for moderately complex tasks.

• Collaborate with internal stakeholders, including Business Units, Business Development, Medical Directors, Business Analysts, and other team members regarding sponsor requirements, protocols, and timelines.

• Conduct research on scientific literature utilizing online resources and internal metrics and tools.

• Assist in the preparation of materials for and participation in bid defense teleconferences and meetings.

• Establish relevant metrics to evaluate protocol feasibility, recruitment support, and site identification and selection efforts.

• Maintain thorough work records and archive pertinent data in internal libraries.

• Aid in the development of feasibility analysis systems and associated metrics.

• Create and sustain systems for the storage, retrieval, and analysis of historical feasibility data for RFPs and RFIs.

• Review, analyze, and present pre-award site-level feasibility assessments through presentations and written reports.

• Engage in the evaluation of informatics technologies, including clinical trial registry searches, enrollment modeling, simulation, and protocol feasibility tools.

• Build and nurture relationships with internal and external stakeholders while supporting study strategies as a subject matter expert.

• May coordinate activities among team members and provide limited mentorship.

• Support departmental management and business objectives.

⛳️ Requirements

• Bachelor’s degree in Science with a focus on medical research.

• Capability to work independently in both virtual and team settings.

• Proficiency in presenting complex scientific and clinical research data as well as analysis methodologies.

• Familiarity with principles, concepts, practices, and standards within the CRO/Pharma industry.

• Effective in sales and bid text development.

• Experience in managing individuals and data to achieve business objectives.

• Strong attention to detail.

• Ability to convert feasibility intelligence into actionable decisions for study and site selection.

• Competence in using historical performance data and market intelligence to inform decision-making.

• Capacity to influence country allocation and site selection strategies through evidence-based recommendations.

• Skills in mentoring and training.

• Advanced proficiency in Microsoft Office Suite, email, and online research.

• Excellent organizational, interpersonal, and team-oriented skills.

• Exceptional verbal and written communication skills in English.

• Outstanding time management abilities with the capacity to handle multiple tasks simultaneously to meet deadlines.

• Flexibility to adapt to change and work collaboratively as part of a team.

• Willingness to travel and adjust work hours as business needs arise.

• Equivalent experience, skills, and/or education may be taken into consideration.

🏝️ Benefits

• Opportunities for career development and advancement.

• Supportive and engaged line management.

• Training in technical and therapeutic areas.

• Recognition among peers.

• Comprehensive total rewards program.

• Inclusive work culture.

• Reasonable accommodations provided when appropriate.