Clinical Research Associate II – Senior Clinical Research Associate
Posted May 10
Posted May 10
This is a fully remote position, open to applicants in Poland.
• You will play a key role in the monitoring activities of clinical trials, taking ownership of your deliverables while working in collaboration with others.
• Conduct site qualification, initiation, monitoring, and close-out visits as part of the clinical trial process.
• Ensure adherence to protocols, maintain data integrity, and prioritize patient safety throughout the duration of the trial.
• Work closely with investigators and site personnel to ensure the smooth execution of the study.
• Engage in data review and resolve queries to uphold the quality of clinical data.
• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.
• A bachelor's degree in a scientific or healthcare-related discipline.
• At least 1 year of experience as a Clinical Research Associate.
• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
• Excellent organizational and communication skills, with a keen attention to detail.
• Capability to work both independently and as part of a team in a fast-paced environment.
• Openness to travel as needed.
• Various annual leave entitlements.
• A selection of health insurance plans to cater to you and your family's needs.
• Competitive retirement planning options to enhance savings and enable confident future planning.
• Access to a Global Employee Assistance Programme, TELUS Health, providing 24-hour support from a network of over 80,000 specialized professionals dedicated to your and your family’s well-being.
• Life assurance coverage.
• Flexible, country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and more.
Gartner
AccessLex Institute
ICON plc
Zonda
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