Site Activation Partner

This is a fully remote position, open to applicants in Canada.

📋 Description

• Facilitate the commencement of clinical trials.

• Ensure adherence to regulatory standards.

• Deliver site start-up and activation tasks to a high caliber.

• Prepare and submit regulatory documents, such as clinical trial applications and ethics committee submissions.

• Coordinate with both internal and external stakeholders to secure approvals and authorizations for study initiation.

• Maintain precise and current records of regulatory submissions and approvals.

• Assist study teams in crafting protocols, informed consent forms, and investigator brochures.

• Engage in study start-up meetings and contribute insights on regulatory requirements and timelines.

⛳️ Requirements

• Bachelor's degree in life sciences or a related discipline.

• Relevant experience in site start-up and activation.

• Previous background in clinical research or regulatory affairs is preferred, but not mandatory.

• Strong attention to detail and excellent organizational abilities.

• Outstanding communication and interpersonal skills, with the capability to collaborate effectively with cross-functional teams.

• Ability to work independently and manage multiple tasks concurrently in a dynamic environment.

• Legal authorization to work in Canada.

🏝️ Benefits

• Competitive base salary with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career paths.