Bilingual Clinical Research Associate (CRA)

Job Title: Bilingual Clinical Research Associate (CRA)

Job Location: Canada, Calgary

Job Location Type: Remote

Job Contract Type: Full Time

Job Seniority Level:

Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Alberta or British Columbia 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 Alberta or British Columbia Canada.

Through our PACE Training Program, you will join otherProfessionals 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!

• 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.

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.

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
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

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.

• 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.

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Originally posted on Himalayas