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Patient Recruitment Coordinator

4 months ago

Baltimore, Maryland, United States Parexel Full time
Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and "first in human" trials are the first step in testing these novel treatments in humans.At Parexel's Baltimore, MD unit our highly trained and skilled Patient Recruitment Coordinator are crucial to ensuring the successful completion of Phase I trials. This role coordinates and assumes responsibility for study participant enrollment, care, and study assignment.Starting your journey with Parexel comes along with an extensive induction program and ongoing training while following your individual career path.What you'll do after training is completed (including but not limited):Screen potential clinical trial volunteers according to protocol specific requirements and CFR/ICH GCP guidelines. Ensure all study laboratory and medical tests are completed and the eligibility requirements specific to assigned studies are metEnsure all established timelines relating to area of responsibility and assigned projects are metEnsure completion of enrollment for assigned studies and manage process closely to minimize wasteEnsure quality control (QC) performance of all electronic and paper source documentsAssist in reviewing Informed Consent Documents, Study Protocols, Source Documents, and Case Report Forms during developmentEnsure screening ratio and marketing expenditures are maintained within study specific budgetParticipate in team project meetings and ensure regular updates for assigned studiesDevelop and present training material to department staff for assigned studiesArrange for pre/post procedure lab work to be performed and initiate follow up as requiredSupport the implementation and application of Clinbase w/n the departmentEnsure follow up to all queries related to screening and enrollment of assigned studiesCollect, organize, and prepare data for physician review. Enter data into database when required. Ensure all paper source documents are completed as required by protocol. Assist physician with completing flow sheets in medical record and progress note. Update and maintain contents of the Clinical Study FileSupport Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure the efficient and compliant clinical operation of the EPCU

​Your Profile:

Bachelor degree required or 3+ years relevant work experience Highly Preferred: Fluent in English and Spanish (written and verbal) OR English and Japanese (written and oral)At least 1-year related experience working in clinical research preferably focused on patient recruitment/enrollment Computer skills and familiarity with research process is required