Clinical Research Associate (Europe) - Talent Pool
Krakow / Bucharest / Brussels / Berlin / LondonFull-Time
Salary not disclosed
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Job Details
- Required Skills
- GCP
Requirements
- minimum 1 year experience + Honours Bachelor Degree (CRA I)
- Minimum 2 years experience + Honours Bachelor Degree (CRA II)
- Minimum 3 years experience + Honours Bachelor Degree (Sr. CRA)
Responsibilities
- Support/conduct (as appropriate) site management through remote and supervised onsite visits (initiation, monitoring, and close-out) in compliance with SOPs, protocol, and GCP.
- Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance.
- Assist/lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle.
- Support/conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support.
- Maintain accurate, timely, and complete TMF documentation, requesting updates as required.
- Provide day-to-day operational support to Senior CRA, and Lead CRAs.
- Participate in training, study meetings, and CRA development activities, building competencies required for role progression.
- Act as subject matter expert, mentor, coach and/or provide performance feedback to manager for peers.
- Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs.
- When required, act as the first escalation point for the resolution of site/patient issues or to address Sponsor concerns.
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