Global Feasibility Lead - Remote & Cross-Border Trials

Syneos Health, Inc.

Rhode Island

On-site

USD 140,000 - 190,000

Full time

4 days ago
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Job summary

Syneos Health in the United States (Rhode Island) seeks a Sr Global Feasibility Lead - Sponsor dedicated to drive pre-award feasibility across UK, Poland, Spain or US. You will independently manage RFP feasibility across indications, coordinate stakeholders, and deliver data-driven site selection and recruitment support.

Strong English, scientific acumen, and MS Office proficiency are essential. The role offers exposure to global sponsors, complex study designs, and opportunities to influence

Qualifications

  • Understanding and presenting complex clinical research data and analysis methodologies.
  • Knowledge of CRO/Pharma industry principles, concepts, practices and standards.
  • Effective sales and bid text development.
  • Ability to translate feasibility intelligence into actionable site decisions.
  • Mentoring and training capabilities.

Responsibilities

  • Leads RFP and paid feasibility objectives across indications with minimal oversight.
  • Manages multiple assignments concurrently and liaises with internal stakeholders.
  • Develops and presents pre-award site feasibility assessments to stakeholders.
  • Supports benchmark of feasibility tools and develops related metrics.
  • Builds relationships with internal/external stakeholders to support study strategies.

Skills

RFP management
Feasibility analysis
Stakeholder management
Data interpretation
Time management

Education

BS/BA in Science

Tools

MS Office Suite
Database applications
Clinical trial registries
Enrollment modeling tools

Job description

Syneos Health in the United States (Rhode Island) seeks a Sr Global Feasibility Lead - Sponsor dedicated to drive pre-award feasibility across UK, Poland, Spain or US. You will independently manage RFP feasibility across indications, coordinate stakeholders, and deliver data-driven site selection and recruitment support.

Strong English, scientific acumen, and MS Office proficiency are essential. The role offers exposure to global sponsors, complex study designs, and opportunities to influence

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