Early Development Clinical Research Associate
Posted May 23
Posted May 23
This is a fully remote position, open to applicants in Germany.
• Performing site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring compliance with protocols, maintaining data integrity, and prioritizing patient safety throughout the trial process.
• Collaborating with investigators and site personnel to ensure the efficient execution of studies.
• Conducting data reviews and resolving queries to uphold the quality of clinical data.
• Assisting 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.
• A minimum of 2 years of experience as a Clinical Research Associate.
• Comprehensive knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Excellent organizational and communication abilities, with a strong attention to detail.
• Capability to work both independently and collaboratively in a dynamic environment.
• Willingness to travel at least 60% of the time (both internationally and domestically) and must hold a valid driver’s license.
• Various annual leave entitlements.
• A selection of health insurance options tailored to meet the needs of you and your family.
• Competitive retirement planning options to enhance savings and prepare confidently for the future.
• Global Employee Assistance Programme, TELUS Health, providing 24-hour access to a worldwide network of over 80,000 independent specialized professionals to support 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, and more.
Parexel
ICON plc
Precision Medicine Group
Worldwide Clinical Trials
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