Clinical Research Associate

📋 Description

• You will play a key role in clinical trial monitoring activities, taking ownership of your deliverables and collaborating effectively with your team.

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

• Ensure adherence to protocol, maintain data integrity, and prioritize patient safety throughout the trial process.

• Work alongside investigators and site personnel to ensure smooth study operations.

• Carry out data review and resolve queries to uphold high standards of clinical data quality.

• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.

⛳️ Requirements

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

• A minimum of 2 years of experience in the role of a Clinical Research Associate.

• Comprehensive understanding of clinical trial processes, regulatory requirements, and ICH-GCP guidelines.

• Excellent organizational and communication skills, with a strong attention to detail.

• Capability to work both independently and collaboratively in a dynamic environment.

• Willingness to travel as needed, approximately 60% of the time.

🏝️ Benefits

• Various annual leave entitlements.

• A selection of health insurance options tailored to meet the needs of you and your family.

• Competitive retirement planning programs to maximize savings and confidently prepare for the future.

• Global Employee Assistance Programme, TELUS Health, providing 24-hour access to a worldwide network of over 80,000 independent specialized professionals dedicated to supporting your and your family’s well-being.

• Life assurance.

• Flexible country-specific optional benefits, such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and more.