Global Feasibility Lead: Strategy & Site Selection

Syneos Health, Inc.

Manchester (NH)

On-site

USD 130,000 - 190,000

Full time

8 days ago

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Job summary

Syneos Health is seeking a Sr Global Feasibility Lead for sponsor-dedicated studies across UK, Poland, Spain or US. You will lead feasibility assessments, coordinate with stakeholders, and drive data-driven site selection to optimize study outcomes.

The role requires strong scientific expertise, excellent English communication, and the ability to manage multiple complex feasibility projects in a fast-paced, global environment with travel as needed.

Qualifications

BS/BA in Science with an emphasis in medical research.
Working independently in a virtual and team environment.
Understanding and presenting complex scientific and clinical research data and analysis methodologies.
Knowledge of principles, concepts, practices, and standards in the CRO/Pharma industry.
Effective sales and bid text development.
Working and managing individuals and data to drive business objectives.
Attention to detail.
Translates feasibility intelligence into actionable study and site selection decisions right sites first time.
Uses historical performance data and market intelligence to support decision making.
Influences country allocation and site selection strategy through evidence-based recommendations.
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.

Responsibilities

Works independently with little oversight towards RFP and paid feasibility objectives across all indications.
Ability to manage multiple assignments of varying complexity concurrently across any therapeutic area.
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 towards personal development objectives 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, visual presentation 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).