Clinical Research Associate

📋 Description

• Executing site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Ensuring adherence to protocols, data integrity, and patient safety throughout the trial process.

• Collaborating with investigators and site personnel to ensure efficient study execution.

• Conducting data reviews and resolving queries to uphold high standards of clinical data quality.

• Assisting in the preparation and evaluation of study documents, including protocols and clinical study reports.

⛳️ Requirements

• A Bachelor’s degree in a scientific or healthcare-related discipline.

• At least 9 months of onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) will be determined by total years of experience.

• 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 collaboratively in a dynamic environment.

• Willingness to travel a minimum of 60% of the time (both internationally and domestically - fly and drive) and possess a valid driver’s license.

🏝️ Benefits

• Various annual leave entitlements.

• A wide array of health insurance options tailored to you and your family's needs.

• Competitive retirement planning options to help maximize savings and confidently plan for the future.

• Global Employee Assistance Programme, TELUS Health, providing 24-hour access to a worldwide network of over 80,000 specialized professionals dedicated to supporting your 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, among others.