Senior Clinical Research Associate
C
ClinChoiceClinical Research CRO
Remote position based in Spain, with Barcelona as the ideal locationFull-TimeSenior
Salary not disclosed
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Job Details
- Languages
- English and Spanish
- Experience
- At least eight (8) years of clinical research experience
- Required Skills
- GCPMicrosoft Office
Requirements
- University Degree in scientific, medical or paramedical disciplines.
- At least eight (8) years of clinical research experience.
- Proven experience as a Clinical Research Associate performing on-site monitoring activities.
- Previous experience working for a CRO.
- Strong knowledge of clinical trial operations and GCP/ICH Guidelines.
- Fluent in English and Spanish.
- Proficiency in Microsoft Office (Word, Excel, Outlook).
- Willingness to travel to clinical trial sites.
Responsibilities
- Support 2–3 clinical trials through site monitoring activities including study start-up.
- Perform site selection, evaluation, initiation, and close-out visits.
- Conduct source data verification and review Case Report Forms (CRF) for quality and completeness.
- Manage investigational products and trial materials to ensure proper supply.
- Coordinate with site staff for timely reporting and follow-up of safety issues like AEs, SAEs, and SUSARs.
- Guide and supervise Clinical Research Associate I staff on the job.
- Collaborate with the Training & Qualification Management Unit to develop training materials.
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