Vikki Hurley
Pharmacovigilance Agreement Consultant
- Role
- Consultant at Biopoint Inc
- Location
- Beaufort, SC, US
- LinkedIn followers
- 500 followers
About Vikki Hurley
Healthcare and legal professional with experience establishing and leading teams responsible for agreements for pharmacovigilance, labeling and product quality and conducting due diligence for pharmacovigilance operations. Practiced in the ability to effectively negotiate and influence to meet company objectives while balancing regulatory and business compliance. Recognized for a strong work ethic, ability to maintain the strictest of confidence, ability to work effectively across many disciplines and establishing relationships both internally and externally. Proven success building pharmacovigilance contracting teams from inception as well as establishing and implementing efficiencies in established organizations. Possess strong writing as well as strategic and analytical thinking skills.
Experience
Consultant
Jun 2023 — Present · US
Currently on assignment at Moderna, Inc. on the Pharmacovigilance Agreements (PVA) Team. Responsible for revising PVA and pharmacovigilance language templates, updating current PVAs, drafting, negotiating and finalization of new PVAs and educating colleagues regarding the importance of PV in collaboration and business partner arrangements.
Education
Penn State University
BSN, Nursing
Temple University - James E. Beasley School of Law
JD, Law
Skills
- Infectious Diseases
- Hematology
- Pharmaceutical Industry
- Sop
- Fda
- 21 Cfr Part 11
- Medical Devices
- Regulatory Affairs
- Lifesciences
- Pharmacovigilance
- Clinical Trials
- Pharmaceutics
- Clinical Development
- Oncology
- Vaccines
- CRO
- Biotechnology
- Drug Development
- Gcp
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