Site Activation Partner

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

📋 Description

• Facilitate the commencement of clinical trials.

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

• Prepare and submit regulatory documents, which include 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 creating protocols, informed consent forms, and investigator brochures.

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

⛳️ Requirements

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

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

• Strong attention to detail and exceptional organizational skills.

• Excellent communication and interpersonal abilities, with a talent for effective collaboration within cross-functional teams.

• Capability to work independently and manage multiple tasks concurrently in a fast-paced environment.

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

• Legal authorization to work in Canada.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• 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.