Global Feasibility Lead II

We are looking for candidates with at least 2 years of experience in the pre-award space. Oncology experience is preferred. If you have strong analytical skills and enjoy collaborating on strategic feasibility assessments for clinical trials, this role offers an exciting opportunity to make a meaningful impact.

Join Fortrea and be part of a team dedicated to advancing global healthcare.

Job Overview: The Global Feasibility Lead II plays a crucial role in operational strategy and planning within the pre-award space. This position involves strategy development, data analysis, and feasibility assessments to support clinical trial planning. The role includes managing global feasibility projects, collaborating across teams to deliver comprehensive reports, and transitioning site selection strategies post-award. Additionally, this position contributes to process improvement, training initiatives, and client interactions related to feasibility findings.

Key Responsibilities:

• Support the development, analysis, interpretation, and presentation of primary and secondary data for operational strategy and planning.

• Conduct data mining of internal and external sources to develop global clinical trial strategies, including country/site mix and enrollment modeling.

• Participate in proposal development and bid defenses, providing data-driven recommendations and identifying potential risks with solutions.

• Collaborate with cross-functional teams to plan and present proposals and bid defenses.

• Serve as a functional reviewer for budgets and proposal text related to feasibility and site identification.

• Lead cross-functional teams in standalone feasibility projects, delivering final reports and recommendations to external clients.

• Contribute to internal and external meetings, presenting feasibility insights and providing training on best practices, processes, and tools.

• Develop and maintain global networking relationships to support feasibility initiatives.

• Lead or contribute to process improvement projects and system enhancements within Feasibility.

• Mentor junior team members as needed.

Required Qualifications:

• Associate degree or equivalent work experience.

• Practical understanding of global drug development and clinical trials.

• Experience in mining, analyzing, and presenting complex scientific data relevant to clinical research.

Experience:

• At least 2 years of industry experience in pharma/biotech, a CRO, or a consulting firm.

Key Skills:

• Strong data mining and analytical skills.

• Excellent writing and presentation abilities.

• High level of professionalism and work integrity.

• Ability to work independently and manage multiple priorities effectively.

• Strong attention to detail and quality control.

• Effective relationship management and negotiation skills.

• Experience analyzing study and investigator performance metrics.

• Self-motivated with the ability to work under pressure.

Technical Requirements:

• Proficiency in Microsoft Office and data compilation tools.

• Knowledge of market analysis tools for therapeutic pipelines.

• Strong data manipulation, reporting, and presentation skills.

• Ability to independently source and analyze scientific/medical data.

What We Offer:

• Competitive compensation and benefits package.

• Professional development and training opportunities.

• Collaborative and inclusive work environment.

• Opportunities for career growth within Fortrea.

Join Fortrea and be part of a dynamic team shaping the future of clinical trials. Apply today to contribute to groundbreaking research and make a difference in global healthcare.

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