Lisa King

About Lisa King

Results‑driven clinical research leader with 25+ years of experience across global CRO environments, specializing in Global Clinical Analytics and Data Management for Phase I–IV clinical trials. Known for leading high‑performing, cross‑functional teams and driving operational excellence through the effective adoption of data standards and best practices.I bring deep expertise in oncology, endocrinology, dermatology, and gastroenterology, paired with a strong track record of delivering complex programs efficiently, compliantly, and with a focus on quality. Passionate about developing talent, optimizing processes, and partnering with stakeholders to translate data into meaningful clinical and business outcomes.

Experience

1. Senior Project Manager, Global Analytics

   Caidya

   Sep 2020 — Present · Raleigh, NC, US

   Senior Project Manager, Global Clinical Analytics, with proven expertise leading cross‑functional teams across Data Management, Biostatistics, Statistical Programming, and Clinical Programming to deliver high‑quality clinical analytics within scope, timeline, and budget. Adept at driving end‑to‑end project execution while ensuring full compliance with SOPs, GCP, ICH guidelines, and applicable regulatory requirements. Recognized as a trusted sponsor partner and primary point of contact, providing clear, proactive communication, risk mitigation, and solution‑oriented leadership to achieve project objectives and maintain strong stakeholder alignment.

Education

• University of Mount Olive

  Bachelor of Science - BS, Health/Health Care Administration/Management

  2020 — 2021

Skills

• Pharmaceutical Industry
• Sdtm
• Crf Design
• Inform
• Electronic Data Capture (Edc)
• CRO
• Standard Operating Procedure (Sop)
• Meddra
• Clinical Data Management
• Oracle Clinical
• Oc Rdc Onsite, Oracle Clinical, Inform, Clin-Trial, Sas, and Rave
• Ich-Gcp
• Cdisc Standards
• Edc
• Ctms
• Cdisc
• Data Management
• Clinical Development
• Medidata
• Gcp