Bilingual Clinical Research Associate (CRA) - Canada

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

This is ahome-based position in Canada.

Through ourPACETraining Program, you will join otherProfessionalsAchievingCRAExcellence 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!

• 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.

• 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.