Senior Clinical Research Associate
Posted Aug 25
Posted Aug 25
This is a fully remote position, open to applicants in Canada.
• Identify, select, initiate, and close investigational sites for phase II–IV clinical trials.
• Set up and monitor studies independently and proactively.
• Complete necessary reports and maintain comprehensive documentation.
• Submit protocol and consent documents for ethics/IRB approval.
• Prepare regulatory submissions as required.
• Manage sponsor-generated inquiries effectively.
• Take charge of study cost efficiency.
• Prepare and review study documentation and feasibility assessments for new proposals.
• Potentially assist in training and mentoring junior CRAs.
• Collaborate with a close-knit team of highly skilled CRAs.
• Ensure compliance with relevant regulations and ICH-GCP standards.
• A minimum of 18 months of monitoring experience in phase I-III trials as a CRA.
• A college degree in medicine, science, or a related field.
• Previous monitoring experience with medium-sized studies, encompassing study start-up and close-out phases.
• Solid understanding of ICH-GCP guidelines.
• Ability to review and assess medical data effectively.
• Excellent written and verbal communication skills in both German and English.
• Capacity to meet tight deadlines.
• Willingness to travel at least 60% of the time, both domestically and internationally.
• Valid driving license.
• Legal authorization to work in the country where the position is located.
• Highly competitive salary packages.
• Annual bonuses based on performance goals.
• Health-related benefits for employees and their families.
• Competitive retirement plans.
• Life assurance coverage.
• Attractive base salary with performance-related incentives.
• Medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career pathways.
• An inclusive and accessible workplace.
• Reasonable accommodations during the recruitment process.
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