6 coding-"https:" "https:" "https:" "https:" "https:" "I.E" positions at University of Pennsylvania
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organization for research publications, with potential for co-authorship. Additional details of these responsibilities are provided below: Coordinate the conduct of complex (i.e., multi-drug regimens, high
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Coordinate, organize and maintain all documentation required by sponsor or Clinical Research Organizations (CROs) (i.e., source documentation, case report forms, study and regulatory binders, and patient
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of our participants and their families. Provide psychosocial support and make suggestions or referrals to other professional staff (i.e. social worker, chaplain) as needed. Intercept and respond
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clinical trials. Coordinate, organize and maintain all documentation required by sponsor or Clinical Research Organizations (CROs) (i.e., source documentation, case report forms, study and regulatory binders
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of our participants and their families. Provide psychosocial support and make suggestions or referrals to other professional staff (i.e. social worker, chaplain) as needed. Intercept and respond
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(I.e., procedures, work instructions, templates). This individual communicates independently at all levels and ensures audit/inspection readiness of assigned projects. The Regulatory Affairs Specialist C