Industry: Healthcare
Type: Full Time
Work Hours: 8
Salary: $20 To $30/An Hour
Location: Canada
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Full job description
clinical trial coordinator jobs remote present an exciting opportunity to join Workvella as a Clinical Trial Coordinator dedicated to advancing clinical research from the comfort of your own space. At Workvella, we connect top Canadian talent with innovative, flexible roles that prioritize work-life balance and career development. As a Clinical Trial Coordinator, you will play a pivotal role in managing and overseeing remote clinical trials, ensuring trials are conducted with integrity, accuracy, and compliance. This role offers not only the chance to impact groundbreaking therapeutic research but also the flexibility and autonomy that come with remote work in a supportive company environment.
Workvella’s mission is to foster a collaborative and innovative professional community by connecting skilled clinical research professionals with meaningful, remote work that fits today’s modern lifestyle. If you are looking for clinical trial coordinator jobs remote that deliver on both career advancement and a healthy work-life balance, this opportunity is designed with you in mind.
Company Profile & Culture
Workvella is a forward-thinking HR and recruitment platform dedicated to connecting Canadian professionals with remote, flexible career opportunities, especially in specialized fields like clinical research. Our culture is grounded in innovation, transparency, and a commitment to support each team member’s growth. We encourage open communication, continuous learning, and a strong sense of community despite working remotely.
At Workvella, we believe that flexibility fuels productivity and satisfaction. Supporting Canadian professionals through flexible remote work options, we champion a culture that values your individual contributions, promotes career development, and respects personal time. Join an organization that invests in your success and understands the evolving needs of today’s workforce.
Key Responsibilities
- Coordinate and manage all aspects of remote clinical trials, ensuring adherence to study protocols, timelines, and regulatory requirements within the context of remote operations.
- Serve as the primary liaison between sponsors, investigators, and clinical sites, maintaining clear and consistent communication remotely.
- Oversee patient enrollment processes and data collection activities through digital clinical research platforms and software such as Medidata and REDCap.
- Ensure compliance with FDA regulations and GCP (Good Clinical Practice) guidelines, performing regular monitoring and quality checks remotely.
- Prepare and manage essential trial documentation, reports, and electronic records to support audits and study close-outs.
- Collaborate with cross-functional teams, including data management and medical affairs, to track study progress and address any issues promptly, all within a remote setting.
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, or related field; relevant clinical research certifications (e.g., CCRC, CCRA) are highly preferred.
- Minimum 3 years’ experience in clinical trial coordination or management, with prior involvement in remote or decentralized clinical trials advantageous.
- Proficient in clinical research software tools such as Medidata, REDCap, and electronic data capture systems, along with strong computer literacy.
- Thorough understanding of FDA regulations, ICH-GCP guidelines, and clinical trial compliance requirements.
- Excellent organizational skills, with ability to manage multiple study activities from a remote environment efficiently and communicate clearly across teams.
- Strong interpersonal and problem-solving skills, committed to maintaining quality and integrity in clinical research.
Benefits & Perks
- Enjoy fully remote work that supports your lifestyle and reduces commuting stress.
- Flexible working hours to accommodate your personal and professional commitments.
- Competitive salary with performance-based incentives.
- Comprehensive healthcare benefits including medical, dental, and wellness programs.
- Access to career development resources, certifications, and training opportunities in clinical research.
- Supportive team culture emphasizing collaboration, transparency, and continuous feedback.
- Generous vacation policy and paid time off to support your work-life balance.
Why Apply for Clinical Trial Coordinator Jobs Remote at Workvella?
If you’re seeking meaningful clinical trial coordinator jobs remote that allow you to contribute to important healthcare research while maintaining a balanced lifestyle, Workvella’s opportunity perfectly matches your ambitions. As a Clinical Trial Coordinator with us, you will benefit from a role designed to maximize your impact while affording you the flexibility and autonomy that modern work demands.
We are committed to your professional growth and will support your continued learning and certification pursuits. Your work will directly influence medical innovations, and you’ll be part of a vibrant, supportive community that values your expertise and fosters your career development. Join Workvella and take your clinical research career to the next level while enjoying the freedom and benefits of remote work.
Apply Now
Don’t miss this chance to secure one of the most sought-after clinical trial coordinator jobs remote available with Workvella. If you are a dedicated and experienced Clinical Trial Coordinator ready to embrace a flexible, remote role that prioritizes both your professional ambitions and personal well-being, we want to hear from you today. Submit your application now and take the first step toward a fulfilling career with Workvella!