Veronica Perry Email & Phone Number

Raleigh, North Carolina, United States

Morrisville, North Carolina, United States

● Conduct thorough eligibility and benefits assessments for patients, collaborating with commercial and governmental insurance companies and pharmacy benefits payers.● Utilize electronic data management systems (EDMS) such as Salesforce to update status reports, logs, and project tracking data, ensuring accuracy and compliance.● Facilitate benefit investigations, specializing in neuroscience medications, and adeptly handle day-to-day activities adhering to regulatory protocols and guidelines.

Morrisville, North Carolina, United States

Description● Verified patient eligibility with commercial insurance companies and pharmacy benefits payers, ensuring adherence to regulatory standards.● Provided expert support for prior authorizations and appeals related to immunology medications. Facilitate submission of necessary documentation for payer/plan review.● Cultivated strong relationships with healthcare providers, promoting trust and collaboration.

Morrisville, North Carolina, United States

● Acted as primary point of contact for various stakeholders including payers, patients, caregivers, specialty pharmacies, and providers, delivering inbound and outbound phone support.● Performed outreach to gather missing information from sites, patients, and field representatives, ensuring comprehensive case resolution.● Facilitated collaborative processes to coordinate patient benefits, product orders, and appointment scheduling. Monitored and tracked benefit investigations and prior authorization cases.● Utilized Salesforce for end-to-end case management, maintaining accurate reporting and escalating complex cases per standard operating procedures (SOPs).

Cary, North Carolina, United States

● Compiled, submitted, and obtained approval of submission documents to Institutional Review Boards (IRB), facilitating the regulatory approval process for clinical trials.● Prepared and reviewed site regulatory documents for clinical trials, ensuring completeness and accuracy while adhering to regulatory standards.● Tracked and monitored progress, approvals, and execution of regulatory documents, including ethics, Informed Consent Forms (ICF), and Investigator Pack (IP) release documents, in alignment with project timelines.● Performed data entry and management in Electronic Data Management Systems (EDMS), maintaining accurate and organized records of regulatory documentation.

Louisburg, North Carolina

● Conducted redeterminations and adjustments for Adult Medicaid program recipients, ensuring compliance with program guidelines and regulations.● Interviewed clients and collateral contacts to gather relevant medical, work, and income history, assessing eligibility based on gathered information.

Bachelors Of Science, Business Administration And Management, General, 3.5

Activities and Societies: Delta Mu Delta

Associate Of Science - As, Medical Office Management/Administration