Research Nurse

Job Category: Biotech/R&D/Science Career Level: Experienced (Non-Manager) Location: Baltimore, MD 21225           Job Description: PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com Essential FunctionExecute and coordinate a variety of specialized clinical research activities ensuring that established protocols are implemented and followed. Monitor patient status and safety. Collects and organizes research data. Educate patients and family members about treatments and possible side effects and complications.RelationshipsReports To Associate Medical DirectorDirectly Supervises noneProvides Work Direction to noneWorks Closely with Physician Investigators, Project Managers, Subject Recruiters, Study Coordinators, , Quality ManagementExternal Relationships Supply, materials and laboratory vendors, clients and project monitors, Auditors, Hospital Clinical Laboratory StaffKey Accountabilities' Support Standard Operating Procedures (SOPs), Good Clinical Practices, and all work processes to ensure the efficient and compliant clinical operation of the CPRU.' Assumes responsibility for patient care and study conduct assignments. Ensures that all study laboratory and medical tests are completed, and that eligibility requirements specific to the assigned study are met. Assesses compliance, symptoms, etc. per study protocol. Arranges for pre/post procedure laboratory work to be performed.' Ensures that all established timelines relating to areas of responsibility and assigned projects are met.' Assesses, monitors, records, and reports patient's condition and reaction to drugs and treatments to the appropriate physician. Dispenses medication as directed (when applicable).' Performs or arranges for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follows GCP quality study documentation.' Collects and prepares data. Organize and enter data into case report forms. Enter data into databases when required. Assists physicians in completing flow sheets in medical records and progress notes. Updates and maintains the contents of the Clinical Study File.' Assists project coordinators and project managers in reviewing informed consent documents, source documents, and case report forms.' Reviews consent forms, treatment schemas, and side effects of drugs with study participants and research team members. Administers Informed Consents according to Good Clinical Practice guidelines. Discusses potential adverse events and study schedules with study participants.' Acts as participant advocate in the conduct of clinical studies.' Performs daily equipment and drug checks as required by departmental policy. Documentation is completed accordingly. Reports equipment failures to the Clinical Services Leader. Arranges for replacement of expired or used supplies in conjunction with the Clinical Services Leader.' Participates and may direct identification and enrollment of study participants. Contributes to the development and implementation of study/research objectives.' Assigns tasks and clinical procedures to appropriately trained research assistants and research technician.' Responsible for clinical trial material accountability in coordination with CPRU Pharmacy Technician and Pharmacist. Maintains security of blinded code and notifies physician of participant conditions, which may require blinded code identification (when applicable).' Supports the implementation and application of ClinBase in the CPRU.' Maintains and participates in the fiscal objectives of the unit and recognizes cost reduction opportunities. Participates in quality improvement initiatives.' Demonstrates Guest and Staff Relations standards in all activities.' Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and is not to be considered as all inclusive Skills ' Excellent organizational and communication skills.' Attention to detail is critical.' Must be self directed and often work with minimal supervision.' Invasive pressure monitoring, emergency care and comprehensive assessment skills are also highly desirable.Education' BSN preferred or relevant work experience.' Licensed LPN, RN, BLS certification.Language Skills' EnglishMinimum Work Experience' At least 1 year related experience.' Computer skills and familiarity with research process is highly desirable.' Working Schedule: As the workflow dictates, will include shift rotation and weekend work, requires on-call obligation with overtime, work schedule may change as business needs dictate.' Physical Requirements: Moving and lifting patient, pushing stretchers, moving heavy monitors, visual and auditory acuity, manual dexterity, exposure to body fluids. RESPOND HERE! Respond immediately by accessing the following dedicated online response form which will allow you to cut and paste your resume. This form will go directly and immediately to the hiring authority for this position. Access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2272102&boardid=749