Global Feasibility Lead

Works independently with little to no oversight towards RFP and standalone paid feasibility objectives

Confidently assesses the level of data and analysis required and proposes approaches for RFPs and individual paid feasibility assessments


Ability to manage an average number of assignments and complexity concurrently
Proactively identifies solutions to non-standard requests

Applies knowledge/skills to a range of moderately complex activities


Independently liaises with internal stakeholders to review sponsor requirements, protocol, and timelines for individual RFPs

Upon discretion of a line manager, may participate in and support activities related to department staff operations


No project oversight expected, some limited mentoring upon discretion of the Line Manager may be expected


May coordinate work of other team members as needed during multi study programs of studies or mentoring period(s)


Supports department management in development of group and achieving business objectives


Liaises with Business Units, Business Development, Medical Directors, Business Analysts, and other members of the team to review sponsor requirements, protocol, and timelines for individual RFPs


Independently manages and performs research of scientific literature using internet and internal metrics and tools to provide background information


May support the preparation of material for and attends bid defense teleconferences and meetings, under review and supervision of a line manager or delegate


Actively participates in developing relevant metrics to measure the impact of protocol feasibility assessments, recruitment support, and site identification and selection activities


Maintains comprehensive records of work and stores all relevant data within internal libraries in a timely manner


May help support development of feasibility analysis systems and support collection of associated metrics

May develop and maintain systems for storage and retrieval and analysis of historical feasibility data in support of current RFPs and RFIs


Review, analysis and delivery of pre-award site level feasibility assessments into presentations and/or written reports for delivery to internal/external stakeholders
May participate in the evaluation of new informatics technologies, such as clinical trial registry search tools, enrollment modeling and simulation tools and protocol feasibility assessment tools


Excellent English verbal and written communication skills


Build and maintain relationships with internal and external stakeholders to develop clear communication methods to support study strategies aimed at becoming the subject matter expert (SME)

Qualifications

What we re looking for
Preferred BS/BA in Science with an emphasis in medical research
Working independently in a virtual team environment with minimum 3yrs of relevant experience
Understanding and presenting complex scientific and clinical research data and analysis methodologies
Knowledge of principles, concepts, practices, and standards in the CRO industry
Effective sales and bid text development
Working and managing individuals and data to drive business objectives
Attention to detail
Mentoring and training capabilities
Advanced Microsoft Office Suite (e

g

, Word, Excel, PowerPoint, database applications), email, and internet research capabilities


Strong organizational, interpersonal, and team-oriented skills
Excellent verbal and written English communication proficiency


Superior time management skills; ability to perform several tasks simultaneously to meet deadlines in a dynamic environment
Ability to be flexible, adapt to change, as well as work collaboratively as part of a team
Must be flexible around travel and work hours if a business need should arise

Travel minimum of 5%