As a SLRC at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs.

What You Will Do:

• The SLRC is required to ensure that meaningful and collaborative scientific exchange through engagement activities is achieved to globally impact our strategies.
• Key to the role is the optimal management of the operations of client’s Investigator Studies Program
• The SLRC manages Congress Operations activity for the TA.

Project Management

• • Project manages and/or supports investigator-initiated studies (ISP), the scientific congresses, and Research & Development (R&D) Congress support for the TA
  • These key functions contribute to the development and refinement of our TA Scientific and Medical Affairs Strategic Plan for Our Company Research Laboratories.
  • Ensures that the oversite of these activities is achieved to globally impact the scientific strategy for TA

Investigator Studies Program

• • Co-leads with ISP
  • Chair (Executive Director of Scientific Affairs) and supports the ISP committee with the review, decision making, and operational management of research proposals
  • Provides optimal oversight of the TA Company ISP operations to ensure that the research submitted by investigators is compliantly and efficiently managed

Congress Support

• • Supports logistical and strategic planning of R&D activities at scientific congresses, such as daily debriefs and scientific leader engagements
  • Co-leads with the EDSA and is planning manager with the EDSA for all disease area scientific engagements.
  • Provides congress support and is responsible for developing and updating the scientific leadership strategy

Required qualifications and experience:

• Bachelor's degree
• 2+ years of pharmaceutical or healthcare-related experience in internal or external scientific research operations
• Strong leadership, project management, and organizational awareness skills
• Strong leadership, resilience, collaborative and interpersonal skills
• Ability to coordinate across divisions
• Ability to lead without direct authority over a continuum of stakeholders
• Research database proficiency
• Experience with Microsoft Office applications

Location:

• United States
• Preference for candidates located in the Pennsylvania region
• Remote role with occasional travel to Upper Gwynedd (UG) as needed

Travel Requirements:

• Travel to scientific congresses approximately 6 times per year

Preferred Qualifications:

• Congress management experience
• Experience supporting scientific engagement activities and stakeholder coordination within Medical Affairs or Scientific Affairs organizations