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 Biotech's, 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 an FSP Associate Feasibility Strategist, you will work directly with a client in their systems and processes.

As an FSP Associate Feasibility Strategist, you will create data driven, high quality insights and modelling to support clinical operations study teams. This role will work in close collaboration with the Protocol Design Lab Director.

Key Responsibilities include, but are not limited to:

• Use internal and industry data sources, along with data analytics, to generate insights used for the planning of clinical trials
• Provide timely, high-quality deliverables (e.g., recruitment plans) to clinical study teams to support clinical trial planning
• Utilization of current and emerging data sources to identify risks and challenges to optimize clinical trial protocol design
• Robust tracking and understanding of assumptions used to generate deliverables
• Drive improvements in operational delivery viability through creating a culture of respectful challenge within the protocol development process
• Identify and share study informatics best practices
• May support the assessment, investigation and utilization of new data analytics and data sources
• May act as Subject Matter Expert for tools and systems
• Maintain information on impact and successes.

Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:

• Industry experience (pharmaceutical R&D or related industry) with direct experience in clinical trials operations, data management, study feasibility or project management/study planning
• Proven track record in problem solving and planning
• Excellent process and project management skills gained in a complex matrix organization.
• Results orientated with a drive to set and reach challenging goals, high standards for performance.
• Excellent influencing and negotiation skills.
• Excellent written and verbal communication skills
• Bachelor’s degree in relevant field (i.e., Data Analytics, Data Science, Computer Science, Life Sciences etc.)

Preferred skills:

• 3+ years industry experience
• Experience utilizing clinical trial recruitment modelling tools
• Experience utilizing industry clinical trial related data sources would be advantageous (i.e., CiteLine, DQS, TriNetX etc.)
• Experience in Oncology and/or Vaccines would be advantageous
• Experience with data manipulation, visualization, or advanced analytics
• Understanding of the drug development process, medical terms, and industry specific classification systems (i.e., ICD-10 etc.) would be advantageous
• High level of proficiency with Microsoft PowerPoint and Microsoft Excel

Working Conditions and Environment:

• Work is performed in an office
• Exposure to electrical office equipment
• 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.

Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.