Cheron Jackson, Ph.D
Ph.D Healthcare Professional with expertise in clinical trial development, regulation and compliance within pharmaceutical and medical device industries
Education
Liberty University
Ph.D, Healthcare Leadership
Thomas Edison State University
M.B.A, Healthcare Management
Thomas Edison State University
Bsc, Technology in Healthcare Services
Experience
Becton Dickison
Clinical Project Manager
• Oversee the planning and execution of clinical studies, including clinical study timeline development, to ensure that deliverables are completed on time and within budget • Develop clinical study protocols, informed consent forms (ICFs), case report forms (CRFs), and other essential clinical study documents • Develop clinical study reports for submission to regulatory authorities • Develop and track the clinical study budget, including invoice review/approval and monthly accruals • Oversee and review deliverables produced by study team members to ensure quality and compliance • Manage external vendors to ensure that deliverables are completed on-time, within budget, and are consistent with the scope of work • Ensure that studies comply with policies, standards and procedures, FDA regulations, ISO standards, Good Clinical Practice (GCP), and other applicable regulations• Interact with investigational sites, vendors, key opinion leaders (KOLs) and consultants
Seqirus
Sanofi
Bristol Myers Squibb
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