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Senior Feasibility Specialist

  1. Mexico City
2024-113697
  1. ICON Strategic Solutions
  2. Patient Recruitment
  3. Remote

About the role

As a Senior Feasibility Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


What you will be doing:

  • Reporting to the Associate Director or Director within FASTR (Feasibility, Activations and Strategy & Tactics of Recruitment), this role will be responsible for providing support to study teams across key programs, to enable acceleration of clinical studies
  • Senior Specialist will play a supportive but critical role in the FASTR Team focusing on the delivery of high quality operational, site feasibility and recruitment deliverables, as needed
  • Works in close collaboration with trial management teams and FASTR study start-up, recruitment and feasibility teams to provide key inputs, metrics, and outputs to support study acceleration strategies for program and protocol planning
  • Supports across a range of rare disease areas and FASTR Feasibility / Recruitment Leads
  • Under the supervision of FASTR Director or Associate Director, supports trial optimization and achievement of study milestones by:
    • Information gathering across multiple data sources and platforms to gain a thorough understanding of therapeutic areas including standard of care, and patient / site profiles
    • Evaluating the trial landscape though data mining and able to interpret and present findings
    • Supporting enrollment forecasting
    • Effectively communicating with study teams and relevant stakeholders as needed to coordinate and support feasibility activities
    • Providing solutions-oriented, creative thinking to maintain administrative tasks related to supporting seamless feasibility execution
  • Working knowledge of clinical trial conduct and direct study/program operations experience with proven evidence of success
  • Excellent organizational, planning, communication, presentation, and interpersonal skills. A self-starter who motivates, has tact, diplomacy and who has a flexible and positive approach.  Ability to work well in novel situations
  • Complete tasks to deadlines and able to prioritize conflicting demands
  • Demonstrated planning and organizational skills including project management

You are:

  • B.S. in a scientific or allied health field (or equivalent degree) and 3+ years of experience demonstrating thorough understanding of clinical trial conduct and processes and/or 2+ years of feasibility/recruitment
    • Degree preferred or equivalent industry experience
  • Demonstrated administrative and project management abilities in an academic, CRO or sponsor environment.
  • Experience working in multiple rare disease therapeutic areas
  • Experience with data analysis and interpretation
  • Highly proficient with excel
  • Excellent verbal and written communication skills; solutions oriented creative thinking

 

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