Cheryl Molnar

Background

About Cheryl Molnar

Highly skilled and accomplished professional with a proven track record in medical coding and pharmacovigilance within the pharmaceutical industry. Committed to ensuring compliance with regulatory requirements, driving operational excellence, and optimizing coding processes to deliver high-quality coding deliverables for clinical trials and programs. Medical Coding | Pharmacovigilance | Regulatory Compliance | Project Management MedDRA and WHO Drug Dictionaries | Clinical Trial Data Management Systems | GCP | FDA Regulations Workflow Optimization | Vendor Management | Team Leadership | Quality Assurance | Problem Solving Key Skills: Medical coding expertise utilizing MedDRA and WHO Drug dictionaries Proven track record in ensuring compliance with regulatory guidelines and GCP Extensive experience in data management, database validation, and risk management Strong project management skills, delivering high-quality coding deliverables Expertise in clinical trial data management systems and FDA regulations Experience Highlights: Driving operational excellence by ensuring compliance and accuracy in coding processes Leading cross-functional teams and managing vendor partnerships Streamlining workflow and optimizing coding practices to enhance efficiency and quality Demonstrating subject matter expertise in MedDRA and WHO Drug dictionaries Contributing to successful database validation initiatives and ensuring data integrity #MedicalCoding #DataManagement #Pharmacovigilance #RegulatoryCompliance #Leadership #QualityAssurance #ClinicalTrials #GCP #FDARegulations #OperationsExcellence