Bilingual Study Start-up Coordinator Canada– Remote

Medpace; Toronto; Remote; CAD 70,000 - 100,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Research Associate in Toronto, Canada. This role involves managing Health Canada submissions and ensuring compliance with regulations. The ideal candidate has a bachelor's degree in a related field and experience in clinical research, including ethics submissions. The position offers competitive compensation, remote work options, and opportunities for professional growth.

Benefits

Competitive compensation and benefits package

Opportunity for professional growth and advancement

Supportive and dynamic team environment

Exposure to diverse studies in innovative therapeutic fields

Remote work option available

Qualifications

• 3-5+ years of clinical research industry experience with Health Canada and Ethics submissions.
• Knowledge of ICH guidelines and applicable local regulations.
• Excellent written and oral communication skills.

Responsibilities

• Serve as the point of contact with sites during the study start-up process.
• Ensure compliance with applicable regulations and guidance documents.
• Track and manage timely filing of all documents related to Health Canada submissions.

Skills

Proficiency in English

Proficiency in French

Organizational skills

Time management skills

Detail-oriented

Education

Bachelor's degree in a science or health-related field

Job description

Pay Competitive

Employment type Other

Job Description

Req#: 7822 Employer Industry: Clinical Contract Research Organization (CRO)

Why Consider this Job Opportunity:

- Competitive compensation and benefits package
- Opportunity for professional growth and advancement within the organization
- Remote work option available
- Supportive and dynamic team environment
- Exposure to diverse and challenging studies in innovative therapeutic fields
- Chance to make a difference in the lives of patients and families facing various diseases

What to Expect (Job Responsibilities):

- Serve as the point of contact with sites during the study start-up process
- Prepare, review, and file clinical trial applications to Health Canada
- Ensure compliance with applicable regulations and guidance documents
- Advise clients on changing regulations and compliance requirements
- Track and manage timely filing of all documents related to Health Canada submissions

What is Required (Qualifications):

- Proficiency in English and French
- Ability to work in a remote setting
- Bachelor's degree in a science or health-related field
- At least 3-5+ years of clinical research industry experience with Health Canada and Ethics submissions
- Knowledge of ICH guidelines and applicable local regulations
- Excellent written and oral communication skills

How to Stand Out (Preferred Qualifications):

- Experience working at a CRO
- Hybrid work-from-home options available
- Strong organizational and time management skills
- Detail-oriented with a focus on accuracy
- Familiarity with Medpace or similar clinical research organizations

#ClinicalResearch #RegulatorySubmissions #RemoteWork #ProfessionalGrowth #InnovativeTherapeuticFields

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About the company

Medpace Holdings, Inc. is a midsize, clinical contract research organization based in Cincinnati, Ohio.

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