A key leadership position serving on the US Medical Affairs Sr. Leadership team, reporting to the VP of US MAF Strategic and tactical lead for Infectious Disease therapeutics (HIV, Hepatitis, RSV) and prevention efforts (COVID, RSV, HIV, and ExPEC)Oversees the Field Medical Affairs strategy for Medical Science Liaisons (MSLs) and Community Liaisons with dissemination of medical information among health care professionals, other key external stakeholders, and the communityOversees the process of obtaining insights and translating to actionable items (i.e. ensuring the creation of high-quality content slide decks, medical presentations at conferences, advisory boards, and insight gatherings, support of R&D and Medical Affairs studies) Led collaboration between US MAF MSLs and JNJ Global Public Health Medical Staff to foster Global Market Expertise Medical Insight Generation for ID pipeline and marketed products as well as vaccines

▪ Contribute to trial design through creation of the PED, protocol, SAP, protocol specific PV criteria, participate in the DSMB/DMC; Answer trial related medical questions and interact with investigators/sites, CROs, etc; Perform medical review and safety analysis of clinical trial subjects; including periodic completion of the Safety Management Plan for individual trials; Assist in the determination whether new safety information requires an Amendment to the CTP and/or ICF; Assess Protocol Violations ▪ Review and approval of “AE coding” and “concomitant medication” lists, Review PV listings, Assist in creation and preparation of the safety part of Top Line Results presentation, CSRs and narratives, abstracts, presentations, and publications; Assist in ADR review and adjudication, Assist in labeling process; Contribute to presentation of trial results▪ Report regularly and work closely with Global Medical Leader, Interact with clinicians/experts (e.g. Advisory boards) as necessary, Act as a support to and resource for Medical Affairs, Assist in the creation of regulatory/submission documents (e.g. clinical summaries, clinical overviews, ASR, IND update)▪ Participation and cooperation in Clinical Team and in other Cross-functional teams, ad hoc, perform medical monitoring on Phase III and Phase IV studies in conjunction with IMPAACT

▪Responsible for various clinical leadership tasks such as providing US clinical perspective on global and publication teams, develop product and disease state strategy, participate in US label discussions and post approval commitments (i.e., Led a Phase IIIb study which led to sNDA approval for the USPI)▪Provide medical input for launch teams, ongoing training for our portfolio and competitor products. (including training, strategy, and development of tools to be used in the field)▪Obtain feedback on company strategy by establishing and maintaining international/national KOL relationships via meetings, advisory boards, and leading speaker training▪Serves as the medical lead for promotional review activities (PRC) to ensure medically accurate and balanced assets to support the brand▪Responsible for data generation activities including the design, protocol development, implementation, and execution of Phase IIIb/IV clinical trials for HIV and HCV (served as SRS a Ph IV HCV study, Ph IIIb PK study in pregnant women, and a Ph I relative bioavailbilty study in healthy volunteers)Served as the Integrated evidence generation lead to create real world evidence (RWE) for payers, integrated delivery networks, KOLs and HCPs by working with external data sources▪Review various CSRs and SAPs, develop and maintain clinical trial strategy that is aligned with marketing strategy, provides strategic feedback to ensure alignment with all regions and to anticipate a change in market dynamics), participates in post IIS approval study interactions with investigators

▪ Responsible for various clinical leadership tasks such as providing US clinical perspective on global and publication teams (CDT, GCT, etc), develop product and disease state strategy, participate in US label discussions and post approval commitments, provide medical input for launch teams (including training, strategy, and development of tools to be used in the field), lead or provide input on presentations at medical and commercial advisory boards (including President’s Council), attend major medical conferences, establish and maintain KOL relationships, train commercial and various MAF teams (including extending MAF teams) on new clinical data, interface with MSL and extended MAF teams (HECOR, Sci Comm/Pubs) on medical strategy, participates in APR discussions, serves as the medical lead for promotional review activities (PRC) for the HIV and HCV disease state and product portfolios (PREZISTA INTELENCE, EDURANT, COMPLERA, and OLYSIO) Responsible for data generation activities including the execution of Phase IIIb/IV clinical trials for HIV and HCV (serve as SRS on SONET and TMC114HIV3015), review various CSRs and SAPs, develop and maintain clinical trial strategy that is aligned with marketing strategy, serve on research calls, participates in post IIS approval study interactions with investigators▪ Serves as clinical lead in various data dissemination activities such as providing a clinical perspective at major medical conferences/pre-cons, delivers presentations at regional clinical meetings, serves as medical lead for PRC, partners with marketing on strategy, slide development, meeting presentations, and training for the promotional speakers bureau, HIV and HCV PAT, med info publication reviews▪ Serves as the PVofficer and ensures that all safety and reporting responsibilities are met, participates in monthly safety and REMS team calls, serves as a liaison between GMS, NA Pharm LSO, and Janssen Therapeutics

 Responsible for ensuring therapeutic area knowledge and leading business process and IT-related initiatives for the SRL team.  Coordinates training and skills assessment initiatives for SRLs, as well as for other Clinical Affairs partners, that concentrate on therapeutic knowledge, integration and application of clinical affairs strategies, and excellence in customer focus. Proactively identifies training needs and maintains training records. Also responsible for therapeutic training and on- boarding of new SRLs and partnerships with sales training Leads and coordinates overall efforts in design and implementation of all therapeutic educational training programs and materials, applying appropriate training and assessment modalities Ensures efficient processes by implementing innovative technologies

 Develop peer relationships with Opinion Leaders and discuss the most current trends and developments in the scientific fields of interest to our customers and Tibotec Therapeutics Facilitate novel unsolicited ideas for Investigator Initiated Studies (Phase IV) in the therapeutic area of interest to Tibotec Therapeutics. Integral support for Company Sponsored Trials ( ex. EAP; GRACE, Pregnancy Study, etc) Provide scientific information/education support by responding to unsolicited requests from HCPs for on and off-label Tibotec Therapeutics product specific inquiries. Identify quality educational program opportunities for furthering the knowledge of disease states relevant to Tibotec Therapeutics. Identify and facilitate new business opportunities and communicate to New Business Development and L & A partners Contribute to scientific competitive intelligence efforts Provide Scientific meeting coverage and meeting report for specific internal J&J partners

 Provided patient and family education on adherence, side effects, drug interactions, correct administration of medications Provided drug information to the clinic team; designed new drug regimens via interpretation of genotype/ phenotype resistance patterns Recorded patients’ drug history and updates to ensure proper drug therapy and follow up Education of clinic staff, pharmacy residents, and students on HIV and adjunct drug therapy Ambulatory: Order entry, filling/checking, triage interventions and dispensing of medication in a high volume community setting.

▪ Assisted with arrangement, preparation and facilitation of multiple courses offered on the Jacksonville campus; Academic Rotation Preceptor▪ College: Pharmacotherapy II & III; Communications, Pharmaceutical Skills Lab▪ Clinical Assistant Professor: Department of Pharmacy, University of Florida▪ Assisted in the organization and case based learning experiences for the third year Jacksonville off-campus pharmacy program; provided review sessions proctored and graded quiz/exams.

ASHP Accredited Pharmacy Specialty Residency

ASHP Accredited Pharmacy Practice Residency