Global Feasibility Lead: RFP & Site Strategy Expert

Syneos Health, Inc.

Muncie (IN)

A distancia

USD 150.000 - 190.000

Jornada completa

Hace 8 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

Syneos Health, Inc. seeks a Sr Global Feasibility Lead to drive sponsor-dedicated feasibility across UK, Poland, Spain or US.

You will conduct independent, data-driven site evaluations, support RFP processes, and collaborate with Medical Directors and Business Analysts to shape trial strategies. You will manage multiple complex assignments, produce actionable insights, and present findings to internal and external stakeholders.

Formación

  • Bachelor-level science degree required with ability to work independently in virtual and team settings.
  • Ability to present complex scientific data and analyses clearly.
  • Experience within CRO/Pharma settings and understanding of feasibility concepts.
  • Proven skills in sales/bid text development and stakeholder communication.

Responsabilidades

  • Works independently on RFP and paid feasibility objectives; assesses data needs and proposes approaches.
  • Manages multiple assignments across therapeutic areas.
  • Liaises with sponsor requirements, protocol, and timelines for RFPs; may support team operations.
  • Mentors or guides junior staff as directed by management; may coordinate team activities in multi-study programs.
  • Develops metrics to measure feasibility impact and supports site identification and recruitment efforts.
  • Maintains records and stores data in internal libraries; supports informatics tools evaluation.

Conocimientos

Independent work style
Excellent English communication
Organizational and team skills
Data interpretation

Educación

BS/BA in Science with an emphasis in medical research

Herramientas

Microsoft Office Suite
Email
Internet research tools

Descripción del empleo

Syneos Health, Inc. seeks a Sr Global Feasibility Lead to drive sponsor-dedicated feasibility across UK, Poland, Spain or US.

You will conduct independent, data-driven site evaluations, support RFP processes, and collaborate with Medical Directors and Business Analysts to shape trial strategies. You will manage multiple complex assignments, produce actionable insights, and present findings to internal and external stakeholders.

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