[Hiring] Associate Director, Clinical Trial Management @Medpace, Inc.

Role Description

Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Clinical Project Directors to join our team in Canada. This is a home-based position in Canada.

• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations.
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables.
• Maintain in-depth knowledge of protocol, therapeutic area, and indication.
• Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided.
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
• Develop operational project plans.
• Manage risk assessment and execution.
• Manage study vendors where applicable.
• Manage site quality and monitoring deliverables.

Qualifications

• Bachelor’s degree in a health-related field required; Advanced degree in a health-related field preferred.
• Experience in Phases 1-4; Phases 2-3 preferred.
• 5+ years as a project/clinical trial manager within a CRO required.
• Management of overall project timeline.
• Bid defense experience.
• Strong leadership skills.

Benefits

• Competitive compensation programs that recognize and reward performance.
• Comprehensive health, wellness, retirement, and PTO benefits.
• Office-based culture with occasional WFH that provides flexibility for eligible positions after training.
• Company-sponsored social events.
• Please note benefits may vary based on country.

Company Description

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.