Associate Director, Clinical Trial Management - Canada

 Posted 5 months ago
  
 Canada
  
5-10 years experience
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AI Summary

Manage day-to-day operations of clinical trials and serve as the primary contact for sponsors regarding project-specific issues. Ensure compliance with ICH/GCP and provide oversight of internal project team members.

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. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular, Renal, Gastrointestinal, Endocrine/Metabolic, Immunology, Inflammation, Infectious Disease, Neuroscience, Ophthalmology and more

 

This is a home-based position in Canada.


Responsibilities

  • 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

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.


Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

 

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

 

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 Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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