As a Site Activation Partner, you will help initiate clinical studies by preparing regulatory documentation and securing essential approvals. Your work will directly support the timely start-up of trials, ensuring adherence to global standards and contributing to the development of new medical treatments.
What You'll Do
- Prepare and submit regulatory applications, including clinical trial authorizations and ethics committee packages.
- Coordinate with internal teams and external partners to obtain required study approvals.
- Maintain accurate records of all submission materials and approval statuses.
- Support the creation of key study documents such as protocols, consent forms, and investigator brochures.
- Contribute to start-up meetings with insights on regulatory timelines and compliance requirements.
Requirements
- Bachelor’s degree in life sciences or a related discipline.
- Demonstrated attention to detail and strong organizational abilities.
- Effective communication skills and experience collaborating across teams.
- Ability to manage multiple priorities independently in a fast-moving setting.
Preferred Qualifications
- Prior experience in clinical research or regulatory affairs is beneficial but not mandatory.
Benefits
- Generous annual leave policies.
- Comprehensive health insurance options tailored to individual and family needs.
- Retirement planning programs designed to support long-term financial goals.
- Access to TELUS Health, a 24/7 global Employee Assistance Programme offering confidential support services.
- Life assurance coverage.
- Flexible, country-specific benefits such as childcare subsidies, bike purchase schemes, discounted gym access, subsidized transit, and wellness assessments.
