Offer summary

Qualifications:

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 with excellent communication skills., Thorough knowledge of clinical trial methodology and regulations..

Key responsabilities:

Conduct pre-study, initiation, monitoring, and closeout visits for research sites.

Maintain ongoing site correspondence and site files.

Complete visit reports and manage study-related databases.

Oversee and interact with clinical research sites and review patient charts.

Job description

Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Canada. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work.

This is a home-based position in Canada.

Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.

WE OFFER THE FOLLOWING

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!

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 maintaining study-related databases;
Oversight and interaction with clinical research sites; and
Review of patient charts and clinical research data.

Qualifications

Bachelor’s degree in science from an accredited university;
At least 1 year 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; and
Proficient in Microsoft Office.

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 5,000 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

Hybrid work-from-home options (dependent upon position and level)
Competitive PTO packages
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Flexible work schedule
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth

Awards

Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

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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