Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking a full-time,
Global Study Start-Up Lead to join our Clinical Operations team in Canada. This position plays a key role in the clinical trial management process at Medpace. With our continued growth in Canada, we are looking for proactive, positive, and self-motivated individuals with a shared commitment to quality to join our supportive and dynamic team.
Incentives can include: competitive bonus program, sign-on bonus, and equity awards.
Responsibilities- Efficiently manage and successfully execute all aspects of global start-up;
- Perform quality checks on submission documents and site essential documents;
- Prepare and approve informed consent forms;
- Serve as a Sponsor point of contact for start-up and regulatory submissions items;
- Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
- Present during bid defenses, general capabilities meetings, and audits
Qualifications- Bachelor's degree in a science or health-related field;
- At least 5 years of study start-up Lead/Manager experience at a CRO;
- Study start-up experience with Health Canada and Ethics submissions;
- Knowledge of ICH guidelines and applicable local regulations; and
- Proficiency in English and French is a plus.
Medpace Perks- Flexible work environment
- Competitive compensation and benefits package
- Life and Medical Insurance
- Voluntary Pension Plan
- Salary set and paid in local currency (CAD)
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
