Clinical Research Assistant

divh2Part Time Clinical Research Assistant/h2pThe Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Essential Responsibilities and Duties:/pulliCreating and maintaining patient charts for all assigned studies./liliPreparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts./liliMaintaining inventory of study specific supplies including lab kits, assessments and participant facing materials./liliTimely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication./liliAssisting Coordinators in assessments, blood pressure, urine collection, draw labs./liliCommunicating with study participants, caregivers, third party vendors and laboratories as needed./liliAssisting Coordinators with scheduling, copying, faxing, and other clerical tasks./liliAiding Coordinators in the facilitation of study monitoring visits./liliCompletion of daily responsibilities delegated by CRC as they pertain to the study and/or participants./liliAssumes other duties and responsibilities as assigned./li/ulpThe above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive. Office/administrative tasks assigned ie: resupplying exam rooms, ordering office supplies, answering phone calls, etc./ppEducation/Experience/Skills:/pulliHigh school graduate or equivalent./liliExcellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.)./liliSkilled in organization and record maintenance./liliStrong personal initiative and attention to detail./liliAbility to clearly communicate both orally and verbally./liliPrior experience in healthcare, research, or clinical settings is a plus./liliBasic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus./li/ul/div