Data Entry Information Management
Resume:
CORNA GOWER
**********@*******.***; Mobile: +1-770-***-****; Roswell, GA
PROFESSIONAL SUMMARY
Detail-oriented healthcare professional with extensive experience in regulatory documentation and patient information management.
Proven ability to ensure accuracy, compliance, and confidentiality across electronic health systems. Adept at working independently in remote environments and collaborating with clinical and regulatory teams to support data integrity and healthcare excellence. WORK EXPERIENCE
MEDICAL ADMINISTRATIVE VOLUNTEER – MAP INTERNATIONAL 11/2023 – PRESENT Remote
Administrative Responsibilities
• Created and maintained patients' treatment lists.
• Managed a desirability scale for the importation of medicine into developing countries.
• Supported the team in reviewing new or complex product offers.
• Handled sensitive health data with care and confidentiality.
• Provided pharmacist input on healthcare and regulatory projects. JOHNSON & JOHNSON (JANSSEN PHARMACEUTICA) 01/1996 – 09/2022 Regulatory Affairs Pharmacist
Key Data Entry & Documentation Responsibilities
• Entered, verified, and maintained regulatory and clinical data across eCTD platforms and document management systems, ensuring accuracy and compliance with global Health Authority standards.
• Managed version control and document integrity, maintaining audit trails to support regulatory transparency and submission readiness.
• Ensured consistency and accuracy of product labeling in alignment with Health Authority requirements.
• Uploaded and indexed Module 1–5 dossier components, harmonizing terminology and formatting across jurisdictions for seamless submissions.
• Conducted quality checks on regulatory documents, identifying and correcting data entry errors to meet technical and compliance specifications.
• Collaborated with healthcare providers and cross-functional teams to clarify documentation, update records, and support regulatory milestones. EDUCATION
• Bachelor of Pharmacy, University of Pretoria, South Africa. Page 2 of 2
SKILLS AND ATTRIBUTES
Core skills
• Data Entry Accuracy: Proven ability to enter, verify, and maintain clinical and regulatory data with precision.
• eCTD & Document Management Systems: Skilled in uploading, indexing, and managing regulatory documents across platforms.
• Version Control & Audit Trails: Maintains document integrity and traceability for compliance and collaboration.
• Microsoft Office Proficiency.
• Quality Assurance: Conducts thorough checks to ensure completeness, consistency, and regulatory alignment.
• Labeling Harmonization: Ensures accurate product information across jurisdictions and submission formats.
• Clinical Trial Documentation: Familiar with handling sensitive trial data and aligning with Health Authority standards.
• Remote Work Readiness: Self-motivated, organized, and experienced in independent, deadline-driven environments.
Professional attributes
• Detail-Oriented: Meticulous in reviewing and correcting data entry errors.
• Confidentiality & Integrity: Trusted to handle sensitive health information with discretion.
• Healthcare Knowledge: Background in pharmacy and regulatory affairs supports clinical understanding.
• Communication Skills: Able to liaise with healthcare providers and cross-functional teams to clarify data.
• Organizational Strength: Manages multiple data streams and documentation workflows efficiently.
• Adaptability: Comfortable working across different systems, formats, and regulatory frameworks.
• Team Collaboration: Supports partnerships and project teams with pharmacist-level insight and documentation support.
VOLUNTEERING
• MAP International – Feasibility study and pharmaceutical/medical projects
• Dream Factory – Fundraising initiatives
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