jamika moore
About
Regulatory & Start-Up Lead, North America at Quintiles; Senior Clinical Trials ... * Reviewed and provided feedback to upper management on project team...
united states
clayton
pharmaceuticals
clinical trials, cro, oncology, gcp, sop, protocol, clinical research, ctms, regulatory submissions, edc, ich gcp, therapeutic areas, biotechnology, endocrinology, infectious diseases, 21 cfr part 11, drug development, immunology, clinical monitoring, regulatory affairs, patient recruitment, fda, pharmaceutical industry, rheumatology, gastroenterology, medical writing, pulmonology, data management, gmp, pharmacovigilance, clinical data management, oracle clinical, clinical development, inform, staff development, tmf, contract negotiation, quality assurance, informed consent, phase ii
Experience
clinical research manager
robert a harrell md rheumatology clinical research
senior clinical trials specialist and team lead
parexel
senior clinical research coordinator
max neeman international
clinical research coordinator
cumberland research associates
healthcare specialist
us army
regulatory and start-up lead, north america
iqvia
jamika moore's Contact Information
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