Site Activation Manager
I
IQVIAClinical Research
Canada, Home-BasedFull-TimeManager
Salary103,000 - 137,280 CAD per year
Apply NowOpens the employer's application page
Job Details
- Experience
- Minimum of 5 years
- Required Skills
- Project ManagementStakeholder management
Requirements
- Bachelor's degree in life sciences or a related field.
- Minimum of 5 years of experience in a scientific or clinical environment.
- At least 2 years of lead experience.
- Demonstrable experience in an international role or equivalent combination of education and training.
- Strong knowledge of regulatory requirements including ICH-GCP guidelines.
- Proven experience in project management, site identification, and selection processes.
- Experience with site contract negotiation and clinical study approvals.
- Proficiency in creating and maintaining project management and tracking tools.
- Ability to mentor and coach team members.
- Excellent communication skills for stakeholder management.
Responsibilities
- Lead strategic planning and project oversight to accelerate site activation using project management best practices.
- Oversee execution of start-up activities and lifecycle maintenance for assigned projects.
- Develop, implement, and maintain Site Activation Management Plans in accordance with the scope of work.
- Collaborate with internal and external stakeholders to ensure project delivery compliance.
- Execute regulatory strategies for clinical study approvals, authorizations, and site contract negotiations.
- Collect and interpret regulatory intelligence to support study submissions and authorization processes.
- Mentor and coach colleagues as required.
- Build and maintain strong relationships with key customers through effective communication and early engagement.
View Full Description & ApplyYou'll be redirected to the employer's site
