Senior Clinical Trial Assistant - Home Based/Canada

PRA Health Sciences; Canada; Hybrid; CAD 60,000 - 80,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Trial Coordinator in Canada. This role includes managing clinical trials, ensuring compliance with regulatory requirements, and collaborating with study teams. The position offers career advancement opportunities, flexible work-from-home options, and a competitive salary with comprehensive benefits.

Benefits

Competitive salary

Comprehensive benefits package

Flexible work-from-home arrangement

Access to global Employee Assistance Program

Various annual leave entitlements

Qualifications

• Minimum 2 years of relevant clinical trial experience.
• Proficient in English, both spoken and written.
• Strong knowledge of regulatory requirements in Canada preferred.

Responsibilities

• Coordinate clinical trials, ensuring compliance with regulatory requirements.
• Prepare and submit IRB/REB applications.
• Maintain documentation in accordance with ICH/GCP guidelines.

Skills

Organizational Skills

Communication Skills

Attention to Detail

Problem-Solving

Education

BA/BS degree in Life Sciences, Nursing, or a related scientific field

Tools

MS Office (Word, Excel, Access, Outlook, PowerPoint)

VeevaVault TMF

Job description

Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Opportunity for career advancement and growth within a leading clinical research organization
- Flexible work-from-home arrangement, allowing for a better work-life balance
- Competitive salary and a comprehensive benefits package including health insurance and retirement planning
- Diverse culture that rewards high performance and nurtures talent
- Access to global Employee Assistance Program for personal and family well-being
- Various annual leave entitlements and optional benefits tailored to your needs

What to Expect (Job Responsibilities):
- Coordinate clinical trials, ensuring compliance with regulatory requirements and timelines
- Prepare and submit IRB/REB applications and manage ICF forms
- Collaborate effectively with multiple study teams across different therapeutic areas
- Maintain thorough documentation and records in accordance with ICH/GCP guidelines
- Work independently while managing multiple trials simultaneously

What is Required (Qualifications):
- BA/BS degree in Life Sciences, Nursing, or a related scientific field, or equivalent experience
- Minimum of 2 years of relevant clinical trial experience
- Proficient in English, both spoken and written
- Strong knowledge of MS Office applications (Word, Excel, Access, Outlook, PowerPoint)
- Excellent organizational and communication skills, with the ability to manage multiple priorities

How to Stand Out (Preferred Qualifications):
- Experience with VeevaVault TMF
- Familiarity with regulatory requirements in Canada, including Health Canada submissions
- Strong attention to detail and ability to work independently
- Previous experience as a study coordinator or research assistant
- Located in the same time zone or able to work regular business hours in the EST zone

#ClinicalResearch #CareerOpportunity #RemoteWork #HealthInsurance #WorkLifeBalance

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