Clinical Research Associate II
Posted May 20
Posted May 20
This is a fully remote position, open to applicants in Spain.
• Conducting site qualifications, initiating, monitoring, and closing out visits for clinical trials.
• Ensuring adherence to protocols, maintaining data integrity, and prioritizing patient safety throughout the trial process.
• Collaborating with investigators and site personnel to ensure the seamless execution of studies.
• Reviewing data and addressing queries to uphold the quality of clinical data.
• Assisting in the preparation and evaluation of study documentation, including protocols and clinical study reports.
• Bachelor’s degree in a scientific or healthcare-related discipline.
• A minimum of 2 years of experience as a Clinical Research Associate.
• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
• Excellent organizational and communication skills, with a keen eye for detail.
• Capability to work both independently and collaboratively in a fast-paced setting.
• Willingness to travel at least 60% of the time (both internationally and domestically - by air and land) and must possess a valid driver’s license.
• 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 confident planning 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 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, among others.
Parexel
ICON plc
Precision Medicine Group
Worldwide Clinical Trials
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