Clinical Research Associate
Posted May 23
Posted May 23
This is a fully remote position, open to applicants in Bulgaria.
• Performing site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring adherence to protocols, maintaining data integrity, and prioritizing patient safety throughout the trial.
• Collaborating with investigators and site personnel to ensure efficient study execution.
• Conducting data reviews and resolving queries to uphold the quality of clinical data.
• Assisting in the preparation and assessment of study documentation, including protocols and clinical study reports.
• A Bachelor’s degree in a scientific or healthcare-related discipline.
• At least 12 months of experience in independent monitoring of clinical sites on-site.
• Prior experience in monitoring clinical trials within the field of psychiatry is beneficial.
• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
• Excellent organizational and communication abilities, with a keen attention to detail.
• Capability to work both independently and as part of a team in a dynamic environment.
• Willingness to travel as necessary (approximately 60%).
• Various annual leave entitlements.
• A selection of health insurance options tailored to meet your and your family’s requirements.
• Competitive retirement planning options designed to enhance savings and enable confident planning for the future.
• Global Employee Assistance Programme, TELUS Health, providing 24/7 access to a worldwide network of over 80,000 independent specialized professionals dedicated to supporting you and your family’s well-being.
• Life assurance.
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and more.
Parexel
ICON plc
Precision Medicine Group
Worldwide Clinical Trials
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