
Clinical Research Associate
Posted 6 days ago

Posted 6 days ago
This is a fully remote position, open to applicants in Spain.
• Perform qualification, initiation, monitoring, and closeout visits at research sites in accordance with the approved protocol.
• Liaise with medical site personnel, including coordinators, clinical research physicians, and other staff members.
• Confirm the qualifications, training, resources, facilities, laboratories, equipment, and personnel of investigators.
• Cross-check medical records and research source documentation with case report form data.
• Notify site staff of entry errors and promote best practices in documentation.
• Report protocol deviations following SOPs, GCP, and relevant regulatory guidelines.
• Ensure that investigators enroll only qualified subjects.
• Review regulatory documentation.
• Oversee accountability and inventory of medical devices and/or investigational products/drugs.
• Verify and assess adverse events, serious adverse events, concomitant medications, and related illnesses.
• Evaluate site patient recruitment and retention, providing suggestions for improvement.
• Prepare monitoring reports and follow-up letters that include summaries of findings, deviations, deficiencies, and recommended compliance actions.
• A minimum of a university degree in a health or life science discipline.
• At least 1 year of experience as a Study Coordinator (SC), Clinical Research Coordinator (CRC), or CRA trainee.
• Willingness to travel approximately 60-80% of the time.
• Proficient in Microsoft® Office and possess general computer skills.
• Exceptional communication and presentation abilities.
• Detail-oriented with strong time management skills.
• Excellent verbal and written communication skills in both English and Spanish.
• Fluency in Catalan will be regarded as an advantage.
• Applications must be submitted in English.
• Comprehensive initial and ongoing CRA training provided through the PACE Training Program.
• Clearly defined CRA promotion and growth trajectory, including opportunities for mentoring and management advancements.
• Competitive salary.
• Potential for significant travel bonuses.
• Office-based environment with on-site mentorship.
• Clearly defined career paths with transparent advancement opportunities.
• Industry-renowned onboarding and training programs.
• Continuous training and opportunities for ongoing learning.
• Comprehensive health, wellness, retirement, and PTO benefits.
• Office-based culture with occasional work-from-home flexibility for eligible positions after training.
• Company-sponsored social events.
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ICON plc
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