Conducted site monitoring visits, ensuring site adherence to study protocols, FDA regulations, ICH-GCP guidelines, ICON SOPs and sponsor-specific policies• Twice received ICON’s Inspire Award for the commitment, hard work and dedication put forth to meet short term deadlines• Thoroughly reviewed and verified site data to reduce data discrepancies, re-training site staff as needed• Reviewed, collected and maintained ISF and TMF regulatory documents • Promptly took action for all protocol deviations identified and escalated deviations as necessary • Reviewed recurring reports sent from study team in a timely manner to ensure site data and regulatory files were in order and took appropriate actions as necessary based on the findings of the reports• Worked closely with study Project Manager in performing inspection readiness activities and writing audit responses

Executed remote site management tasks in accordance with SOPs and the study monitoring plan, actively addressing specific site needs and ensuring timely data management• Acknowledged with ICON’s Inspire Award for exceptional reception of client feedback.• Primary contact for clinical research trial sites; provided assistance in query resolution and request handling• Performed quality review audits of the study’s eTMF• Communicated with clinical sites for enrollment updates, data entry compliance and sponsor-specific tasks

Coordinated multiple clinical research trials simultaneously under the direction of the principal investigator, ensuring adherence to FDA regulations, ICH-GCP guidelines and sponsor-specific policies• Executed multiple clinical research trials simultaneously, from subject recruitment to end of trial• Facilitated the completion of clinical charts and case report forms• Collected clinical data, reviewed medical records and identified and reported adverse events• Performed ECGs and obtained vital signs of patients• Handled serious adverse effects (SAE) Reporting• Maintained regulatory documents and submitted documents to Institutional Review Board as needed

Short-term contract role locating and enrolling participants for a COVID-19 treatment clinical research study• Independently developed a nationally implemented clinical research recruitment strategy that creatively identified and connected with potential clinical research subjects within the community• Delivered educational presentations across the community with the aim of boosting study referral rates

Filled and dispensed prescriptions in a retail pharmacy under the supervision of a licensed pharmacist• Won SpotRx’s inaugural recognition award via pharmacists’ nomination for consistently demonstrating the best work ethic and delivering high-quality performance of any pharmacy technician they had worked with at SpotRx Pharmacy• Filled prescriptions• Insurance billing• Completed customer sales transactions• Managed inbound patient calls in a timely manner using proprietary audio/video technology

Responsible for increasing usage and awareness of SpotRx’s pharmacy kiosk with patients and clients• Navigated patients through the virtual prescription dispensing process of the kiosk• Built strong relationships within the clinic to bring awareness and educate site staff of kiosk use • Proactively approached customers to provide information about the kiosk services

Coordinated workshops to assist older adults who may be at risk of developing Mild Cognitive Impairment via educating them and referring them into local clinical research studies. • Won inaugural ICARE Award for Innovation, Compassion, Advocacy, Respect, Excellence• Performed educational presentations, taught participants how to perform Cogniciti’s Brain Health Assessment and reviewed participants’ reports upon completion for risk of MCI• Referred participants into local clinical research studies upon confirmation of interest and eligibility

Coordinated multiple clinical research trials simultaneously under the direction of the principal investigator, ensuring adherence to FDA regulations, ICH-GCP guidelines and sponsor-specific policies• Executed clinical research trials from subject recruitment to end of trial• Ran reports from PI’s patient database to find potential subjects and prescreened them for eligibility. Scheduled subjects if qualified and interested. Documented all information via CTMS system

Coordinated multiple clinical research trials simultaneously under the direction of the principal investigator, ensuring adherence to FDA regulations, ICH-GCP guidelines, and sponsor-specific policies• Executed multiple clinical research trials simultaneously, from subject recruitment to end of trial• Facilitated the completion of clinical charts and case report forms• Collected clinical data, reviewed medical records and identified and reported adverse events• Maintained regulatory documents and submitted documents to Institutional Review Board as needed

Assisted in coordination of clinical research trials by performing entry-level duties under the direction of the principal investigator, ensuring adherence to FDA regulations, ICH-GCP guidelines, and sponsor-specific policies• Facilitated the completion of clinical charts and case report forms• Collected clinical data, reviewed medical records and identified and reported adverse events• Performed ECGs and obtained vital signs of patients• Obtained blood specimens using venipuncture technique

Conducted participant outreach to qualify and enroll prospective participants who have been identified through data analysis to likely benefit from chronic disease prevention and control programs while explaining program benefits and services.

Under direct supervision of the President of Viridian Health Management, assisted in research and enrollment for the purpose of company growth to implement evidence-based workplace wellness programs within small and mid-sized employers supported by community-based resources.