Clinical Research Associate

This is a fully remote position, open to applicants in Switzerland.

📋 Description

• You will play a key role in clinical trial monitoring activities, taking ownership of your deliverables and engaging in collaborative efforts.

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

• Ensure compliance with protocols, maintain data integrity, and prioritize patient safety throughout the trial process.

• Work alongside investigators and site personnel to ensure seamless study execution.

• Review data and resolve queries to uphold the quality of clinical data.

• Assist 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 2 years of experience as a Clinical Research Associate.

• 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 fast-paced setting.

• Openness to travel as necessary (approximately 60%).

🏝️ Benefits

• Various annual leave entitlements.

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

• Competitive retirement planning options to enhance savings and confidently prepare for the future.

• Access to the Global Employee Assistance Programme, TELUS Health, providing 24-hour support from a network of over 80,000 independent specialized professionals for 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.