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Charlene Abrams

Associate Director, Global Trial Leader @Johnson & Johnson Innovative Medicine

Abington, PA, US
EMAILS
[email protected]
MOBILE NUMBERS
+12•••••••72

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WORK HISTORY

Dec 2017 — Present

Associate Director, Global Trial Leader @Johnson & Johnson Innovative Medicine

EDUCATION

2001 — 2004

Temple University

M.S., Quality Assurance and Regulatory Affairs

N/A

CHEYNEY UNIVERSITY

B.A, Biology

SKILLS

Phase IClinical TrialsClinicalRegulatory SubmissionsPharmaceutical IndustryFdaClinical ResearchClinical PharmacologyPharmacokineticsHematologyBiotechnologyDrug DevelopmentMedical WritingRegulatory AffairsLifesciencesImmunologyCROClinical DevelopmentNeuroscienceBiomarkersGlpPharmacologyCtmsMedicineOncology

ABOUT CHARLENE ABRAMS

Highly motivated, results oriented Clinical Professional with extensive pharmaceutical industry experience that spans preclinical drug discovery through Phase 4 research. Interfaced well with all levels of staff to achieve maximum results. Exceptional capacity to manage numerous projects with ease.Specialties-Regulatory knowledge of current federal guidelines/regulations; Oversaw daily activities with CRO and investigator site communications; Management of clinical grant budgets and Investigator/CRO/other vendors\' payments; Coordinated Request For Proposal Process (RFP); Coordinated Study Start Up and Close Out Activities; Coordinated Investigational Supplies; and Conducted Study Team Meetings.

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