YOUR CONTRIBUTION
As Clinical Project Associate (m/f/d) you support the conduct of Merz Therapeutics sponsored clinical trials to ensure adequate quality and meet regulatory and legal requirements. Your detailed tasks are the following:
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Support selection, qualification and training of external providers and clinical trial sites
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Oversight of operational tasks of vendors
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Review of monitoring activities and occasional co-monitoring site visits
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Support preparation and review of trial-specific documents, e.g., Informed Consent Form, Operational Plans, site-specific templates
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Maintenance and quality checks of eTMFs to ensure readiness for audits and inspections
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Coordination of internal and external team meetings including writing of minutes
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Maintaining trial databases and supporting internal status reporting
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Contribute to audits and management of CAPAs