High performing, strategic thinking professional with more than eight years' experience in clinical research in the industry, nonprofit and higher education sectors. Highly skilled at relationship building with clinical research collaborations across departments and teams; exceptional writing, presenting, and interpersonal communication skills. Adept at assessing needs, generating options, and implementing solutions in collaboration with pharmaceutical, medical device and internal clients and stakeholders. Well versed in all phases of clinical research, including defining departmental and patient needs, assessing
needed resources and evaluating successful study initiation outcomes. Experienced at managing projects from the start-up and study initiation through to completion and study close out.
PhD dissertation - To be determined.
Society of Clinical Research Associates (SOCRA)
Budget, Contracts, Informed Consent, Good Clinical Practice, Institutional Review Board, FDA, NIH, Community outreach, Clerical/Adminstrative, scientific conferences, Data collection and analysis, Protocol implementation, Patient recruitment, reporting, Risk management, specimen collection, analysis and shipment, AE/SAE reporting, vitals,
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