Site Activation Partner

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

📋 Description

• Execute site start-up and activation tasks to an exceptional standard.

• Aid in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.

• Collaborate with internal and external stakeholders to secure approvals and authorizations for the initiation of studies.

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

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

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

⛳️ Requirements

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

• Prior experience in clinical research or regulatory affairs is preferred but not mandatory.

• Exceptional attention to detail and strong organizational skills.

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

• Ability to work autonomously and juggle multiple tasks simultaneously in a dynamic environment.

• Willingness to travel as necessary (approximately 5%).

• Legal authorization to work in Canada.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, which may include medical, dental, and vision coverage.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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