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Research Site Monitor Professional

1 week ago


Toronto, Ontario, Canada Medpace Full time

**About Medpace:**

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

Our Mission:

To accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.

About the Job:

We are seeking a Clinical Research Associate to join our team in Canada. This is a home-based position that requires traveling between 60-80% of the time.

Responsibilities:

  • Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
  • Maintain ongoing site correspondence and site files;
  • Complete visit reports and maintain study-related databases;
  • Oversight and interaction with clinical research sites;
  • Review of patient charts and clinical research data.

Requirements:

  • Bachelor's degree in science from an accredited university;
  • At least 1 year of experience as a Clinical Research Associate or Clinical Research Coordinator;
  • Bilingual in English and French;
  • Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations;
  • Excellent interpersonal, written and verbal communication skills in English and French;
  • Strong attention to detail and organization skills;
  • Highly motivated, independent, flexible;
  • Ability to travel between 60-80%;
  • Ability to prioritize workload to meet timelines across multiple studies;
  • Proficient in Microsoft Office.

What We Offer:

  • Competitive bonus plans including Resourcing Bonus (following training completion and successful assignment to studies) and Yearly Travel Incentives;
  • Voluntary retirement scheme;
  • Home office furniture allowance, mobile phone and hotspot for internet access anywhere;
  • In-house travel agents, reimbursement for airline club and TSA pre-check;
  • Customized PACE training program based on your experience and therapeutic background and interest;
  • User friendly CTMS with electronic submission and approval of monitoring visit reports;
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
  • National assignments with average of 2 protocols;
  • In-house administrative support for all levels of CRAs;
  • Opportunities to work with international team of CRAs;
  • Low turnover rates for CRAs;
  • No metric for minimum required days on site per month;
  • Flexible work hours across days within a week;
  • Opportunity for CRA leadership positions – Lead CRA, CRA Manager;
  • Many additional perks unmatched by other CROs.