Catalyst Clinical Research - Raleigh, NC

posted 27 days ago

Full-time - Mid Level
Raleigh, NC
Administrative and Support Services

About the position

The Feasibility Manager at Catalyst Clinical Research LLC is responsible for producing feasibility proposals and reports for both pre-award business development activities and post-award ongoing studies. This role involves setting priorities for workload and deliverables, coordinating activities with stakeholders, and ensuring data integrity in feasibility proposals. The manager will also represent the company in bid defense opportunities and participate in internal meetings.

Responsibilities

  • Research, compile and analyze therapeutic area(s) information contained in the clinical protocol.
  • Collect and analyze metric-based global intelligence for pre-award strategic clinical trial development.
  • Collaborate with medical experts on trial conduct and proposed therapy acceptance in target regions.
  • Responsible for recruitment rate & enrollment data verification and proposal text generation.
  • Conduct independent standalone site outreach projects as required.
  • Interact with sites, clients, vendors, and advocacy groups as a secondary project contact.
  • Review clinical protocols, study assumptions, and client information for US and global trials.
  • Provide input to proposals and business development activities to help build project assumptions, budget, and timelines.
  • Present and explain feasibility analysis to BD/Clients in both verbal and written formats.
  • Manage time and project requirements based on study contract.
  • Design site surveys/questionnaires to obtain key information.
  • Arrange the post-award handover to Site Activation Manager.

Requirements

  • Master's or PhD in a scientific field or comparable advanced scientific/clinical degree (e.g., PharmD).
  • 3 years of relevant experience in drug development with 2-4 years in pre-award feasibility and post-award site selection.

Nice-to-haves

  • Experience using external Clinical Trial Databases (e.g., Informa Citeline, TriNetX, PubMed/Medline).
  • High data analysis competency and ability to develop complex models using MS Excel.

Benefits

  • Flexible working conditions (office or home based).
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