Site Activation Partner

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About the role

  • Site Activation Partner launching clinical trials for ICON’s sponsor-dedicated research programs. Coordinating regulatory submissions, approvals, and study-startup documentation.

Responsibilities

  • Deliver site start-up and activation work to a high standard
  • Assist in preparing and submitting regulatory documents, including clinical trial applications and ethics committee submissions
  • Coordinate with internal and external stakeholders to obtain approvals and authorizations for study initiation
  • Maintain accurate and up-to-date records of regulatory submissions and approvals
  • Support study teams in developing protocols, informed consent forms, and investigator brochures
  • Participate in study start-up meetings and provide input on regulatory requirements and timelines

Requirements

  • Bachelor's degree in life sciences or a related field
  • Previous experience in clinical research or regulatory affairs preferred, but not required
  • Strong attention to detail and organizational skills
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams
  • Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment
  • Willingness to travel as required (approximately 5%)
  • Legal right to work in Canada

Benefits

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Job type

Full Time

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

RemoteCanada

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