Zach Eades

About Zach Eades

Experienced research professional with a demonstrated history of working in the pharmaceuticals industry. Skilled in Clinical Operations with a BS focused in Biology from The University of Kentucky and a Master\'s in Health Sciences.I work with biopharmaceutical and medical device companies who need medical affairs, regulatory affairs, and clinical operations expertise to accelerate approval of their drug and/or device. In my role at Medpace, I work with sponsors to understand their clinical study/program requirements including budgets, timelines, and geographies, and respond with proposals that will deliver the greatest value.You can contact me directly at z••••••@medpace.com to learn more.Therapeutically Focused and MetabolicGastroenterologyGeneral SurgeryHemodialysisHemodynamicsInfectious Disease and VaccinesIntensive CareNephrologyNeuroscienceOncology and HematologyOphthalmologyOrthopedicsSpinalVascular DiseaseWomen\'s HealthWound CareSpecialties:Regenerative MedicineRare Disease/Orphan DrugPediatrics

Experience

1. Director, Business Development

   Medpace

   Oct 2021 — Present · Cincinnati, OH, US

   Responsible for the execution of marketing, sales and public relations plans; developing and managing customer relationships; and generating new Phase I-IV CRO, Lab and medical device trial services sales opportunities.Medpace is a full-service Clinical Research Organization (CRO) known for its therapeutic and regulatory excellence in drug and medical device clinical development. We build strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to approval.

Education

• University of Kentucky

  BS, Biology

  2006 — 2008

• Morehead State University

  Bachelor of Science (BS), Biology

  2004 — 2006

• Northern Kentucky University

  Master of Science - MS, Health Sciences

Skills

• Pharmacovigilance
• Ich-Gcp
• Patient Recruitment
• Clinical Development
• Medidata
• Good Clinical Practice (Gcp)
• Inform
• Institutional Review Board (Irb)
• Electronic Data Capture (Edc)
• Diabetes
• Regulatory Submissions
• Irb
• Biotechnology
• CRO
• Clinical Data Management
• Oracle Clinical
• Infectious Diseases
• Drug Development
• Gcp
• Clinical Monitoring
• Clinical Trial Management System (Ctms)
• Clinical Research
• Clinical Pharmacology
• Data Management
• Clinical Research Associates
• Clinical Operations
• Regulatory Affairs
• Medical Writing
• Oncology
• Edc
• Therapeutic Areas
• Protocol
• Ctms
• Cardiology
• CRO Management
• Clinical Trials
• Pharmaceutical Industry
• Sop
• Hypertension