Jose MacIas
President at Visionary Investigators Network
- Role
- Senior Director of Clinical Research at Visionary Investigators Network
- Location
- Miami, FL, US
- LinkedIn followers
- 500 followers
About Jose MacIas
Current Director of Clinical Operations at Visionary Investigators Network, an organization where I\'ve been utilizing my overall knowledge in the clinical research industry to maintain high standards and quality of phase I, II, and pharmaceutical clinical trials. Leading a well-versed team of individuals with vast experience and specialties in multiple areas in the business, from a well-defined Recruitment Department, concise Quality Assurance & Quality Control Plans, a Compliant Regulatory Department, and effective Screening and Conduct practices.
Experience
Senior Director of Clinical Research
Visionary Investigators Network
Apr 2017 — Present · Miami, TX, US
Clinical research management with emphasis in Phase I, II & Clinical Studies. Responsibilities include- Ensure that all required resources are available to conduct successful clinical trials by adhering to Standard Operating Procedures, GCP, & IRB regulations- Management of all daily operations of clinical site, including study conduct, personnel management, and financial and budget management- Provide logistical and feasibility decisions to conduct clinical studies- Ensure adequate staff training to meet quality standards and forecasted workloads- Represent organization on client meetings to develop the business.
Education
Florida Atlantic University
Business Administration and Management, General
2002 — 2008
Skills
- Quality Assurance
- Clinical Data Management
- Good Clinical Practice (Gcp)
- Therapeutic Areas
- CRO
- Regulatory Submissions
- Ctms
- Gcp
- Clinical Pharmacology
- Oncology
- Pharmaceutics
- Training
- Fda
- Cross-Functional Team Leadership
- Ich-Gcp
- Infectious Diseases
- Medical Writing
- Pharmaceutical Industry
- Phase I
- Validation
- Biotechnology
- Clinical Development
- Electronic Data Capture (Edc)
- Regulatory Affairs
- Edc
- Clinical Trial Management System (Ctms)
- Clinical Monitoring
- Standard Operating Procedure (Sop)
- Drug Development
- 21 Cfr Part 11
- Clinical Trials
- Clinical Research
- Protocol
- Data Management
- Medical Devices
- Clinical Operations
- Sop
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