Clinical Research Associate

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

📋 Description

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

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

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

• Work in partnership with investigators and site personnel to ensure smooth execution of studies.

• Engage in data review and resolve queries to uphold high-quality clinical data standards.

• 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.

• At least 2 years of experience working 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.

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

• Willingness 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 ensure confidence in future financial planning.

• Access to the Global Employee Assistance Programme, TELUS Health, providing 24/7 support from a global network of over 80,000 independent specialized professionals for you 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.