
Associate Feasibility Strategist
Wilmington, NCJobSeen todaySeen in employer's feed today
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Job overview
The Associate Feasibility Strategist leads feasibility assessments for clinical programs and trials within a therapeutic area, translating protocol requirements into data-driven insights and country- and site-level intelligence. The role drives cross-functional feasibility strategies and supports decisions on trial planning, country and site selection, and operational study design. The posting seeks relevant pharmaceutical industry experience and two years of feasibility-specific experience; an advanced degree is preferred.
Skills & qualifications
Skills
Qualifications
Full job description
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as Associate Feasibility Strategist – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As Associate Feasibility Strategist, you will lead end-to-end feasibility assessments for clinical programs and trials within a therapeutic area. You will enable informed decisions on trial planning, country and site selection.
What You’ll Do:
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Lead end-to-end feasibility assessments for clinical programs and trials within a therapeutic area
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Translate protocol requirements into data-driven feasibility insights with country- and site-level intelligence
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Drive feasibility strategies across functions, collaborating with Medicine, CDOLs, Country Feasibility Managers, and Data Operations
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Address planning challenges and ensure operational feasibility of study designs
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Enable informed decisions on trial planning, country and site selection, supporting timely, cost-effective, and high-quality execution
Education and Experience Requirements:
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Advanced degree preferred, can consider BS in a medical, public health, life sciences, biostatistics, data science, or related field, with relevant 5+ years of pharmaceutical industry experience
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Two years of feasibility specific experience required
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Expertise in leveraging clinical and real-world data to inform feasibility assessments and site selection
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Proficiency in applying advanced analytics and technology to optimize trial planning and operation
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Oncology experience is a plus
Knowledge, Skills and Abilities:
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Good judgment and decision-making skills
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Thorough attention to detail
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Capable of analyzing data to make good decisions
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Capable of working both as a team player and independently
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Good leadership skills as shown through management of a project with cross-functional and client interaction
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Good oral and written communication skills
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Good multitasking skills to manage multiple projects simultaneously
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Good understanding of confidentiality and data privacy requirements
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Basic understanding of budgeting and forecasting, and managing to contractual expectations
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Good computer skills
Working Conditions and Environment:
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Work is performed in an office
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Exposure to biological fluids with potential exposure to infectious organisms
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Exposure to electrical office equipment
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Exposure to electrical office equipment.
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Long, varied hours frequently required
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Travel may be required
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
How this job compares
Set against the 1,299 open Clinical Research jobs on Olive Jobs, counted November 15, 2026.
- Pay
- This postingNot listed
- North Carolina median$82–220K/yr34 salary ranges
- US median$26–36/hr180 hourly ranges
- Openings
- Olive Jobs lists 61 open Clinical Research jobs in North Carolina and 1,299 across the US. 10% of them nationwide are listed as remote or flexible.
- Hiring the most in North Carolina
- IQVIA30 open
- ThermoFisher Scientific (this employer)14 open
- Advocate Health3 open
- Experience
- This posting asks for at least 2 years of experience; Clinical Research postings that state a minimum ask for 3 years at the median (1,014 postings).
- Education
- 545 of the 1,299 open Clinical Research jobs (42%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 15, 2026. Figures based on too few postings are left out.
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