Clinical Research Coordinator | Cancer Center | PRN

Work Status Details PRO RE NATA - AS NEEDED | 16.00 Hours Every Two Weeks Shift: Days Pay Rate Type: Hourly Location: Cancer Center Salary Range Listed is the base hiring salary range offered for this position. Actual salaries may vary depending on factors, including but not limited to skills and experience. The salary range listed is just one component of the total rewards/compensation package offered to candidates. Min = $30.11 Mid = $37.63 Max = $45.16 Overview The Clinical Research Coordinator coordinates with Principal Investigator (PI) and study team to help ensure that clinical research and related activities are performed in accordance with federal regulations and YRMC institutional policies. This individual requires strong interpersonal skills, ability to communicate with patients regarding study risks and benefits, ability to educate patients, compassion and a desire to help people and uses strong communication skills, organizational skills, attention to detail. The Clinical Research Coordinator is responsible for the efficiency and accuracy of clinical studies through all stages as the study progresses and show vigilance in participant safety, protocol compliance, and data quality. Responsibilities Conducts all delegated research related activities in compliance with the protocol, institutional policies, good clinical practice, FDA, OHRP, and HIPAA policies. Supports Clinical Research Regulatory Coordinator and the study team in the maintenance of regulatory documents in accordance with Standard Operating Procedures (SOP). Develops accurate source materials and ensures compliance from study team. Assist with the maintenance of subject logs, research charts and study binders. Evaluates patient records for enrollment in clinical research studies following ethical practices and institutional policies. Monitors the study to ensure that it complies with protocols, is ethically conducted and follows regulatory standards. Coordinates and/or performs a variety of procedures/tests including, but not limited to, laboratory tests/phlebotomy, vital signs, ECG/EKGs, imaging studies, questionnaires/evaluations, as well as other needs as outlined in the study protocol(s). In accordance to job scope, delegation and responsibilities participates in the protocol specified study visit activities. Assures collection, labeling, processing, storage and shipment of any protocol-required samples for local or central laboratory analysis. Maintains study supply inventory to include accountability and dispensing records. Resolve research data queries within the SOP guidelines, Sponsor protocol and contract requirements. Participates in periodic visits from sponsor, regulatory authorities and other agencies. Other duties as assigned. Minimum Education and Experience Required Bachelor’s Degree in Health Science or related field 2+ years related in interventional clinical research trials BLS (AHA BLS Certification should be achieved within 6 months of role) Research Certification in SOCRA, ACRP, CHC or CHRC (Certification should be achieved within 3 years in role) Competency in Phlebotomy, Vitals, EKG, Point of Care Testing (POCT) (Competency should be achieved within 6 months of role) Preferred Education and Experience Certified Medical Assistant Bilingual in Spanish and English Physical Requirements and working conditions for this position will be provided to you up on interview. #J-18808-Ljbffr