Remote Study Start-Up Project Manager - Canada

 Posted 3 hours ago
  
 Canada
  
5-10 years experience
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AI Summary

The Project Manager will efficiently manage and execute all aspects of global study start-up, including performing quality checks on submission documents. They will also serve as the primary Sponsor point of contact and present during bid defenses and audits.

Our 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 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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