Clinical Research Coord Assoc

Mission StatementMichigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.Mission AlignmentThis position supports the mission of Michigan Medicine to advance health through outstanding clinical care, education, and research. The Clinical Research Coordinator (CRC) will directly contribute to cutting-edge infectious diseases and critical care research by coordinating NIH/NIAID - and STRIVE-funded studies that address severe pneumonia and respiratory infection outcomes.Why Join Michigan Medicine?Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in . Michigan Medicine is comprised of over 30, employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world’s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.What Benefits can you Look Forward to?Excellent medical, dental and vision coverage effective on your very first day 2:1 Match on retirement savingsResponsibilities*Expert level knowledge, skills, and abilities within all 8 competency domains is expected:Scientific Concepts and Research DesignEthical Participant Safety ConsiderationsInvestigational Products Development and RegulationClinical Study Operations (GCPs)Study and Site ManagementData Management and InformaticsLeadership and ProfessionalismCommunication and TeamworkOther responsibilities include:Coordinate daily study activities, including screening, enrollment, informed consent, and data and biospecimen collection.Maintain accurate and timely data entry in REDCap.Serve as liaison between investigators, ICU clinical teams, laboratory staff, and sponsors.Prepare and maintain IRB and sponsor regulatory submissions and ensure compliance with Good Clinical Practice (GCP).Coordinate biospecimen collection, processing, and shipment in collaboration with laboratory teams.Conduct data verification, resolve queries, and ensure data integrity for sponsor audits.Participate in study meetings, teleconferences, and site monitoring visits.Assist in preparing progress reports, manuscripts, and conference materials related to study findings.Supervision Received: This position should report directly to a Clinical Research Coordinator Lead, Clinical Research Project Manager, Administrator, or Faculty Principal Investigator.Supervision Exercised: None initially. Required Qualifications*Bachelor's degree in Health Science or an equivalent combination of related education and experience is necessary.Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to register or take the exam at date of hire, and the certification must be competed or passed etc. within six months of date of hire. (Please review eligibility criteria from Minium 2 years of directly related experience in clinical research and clinical trials is necessary.Knowledge of research regulations, IRB procedures, and GCP standards.Strong organizational and interpersonal communication skills.Proficiency in Microsoft Office, REDCap, and electronic medical records (e.g., MiChart/Epic).Desired Qualifications*4+ years of direct related experience.Certification as a Clinical Research Coordinator (CCRC) or equivalent.Experience with NIH-funded or multicenter clinical trials.Experiencing working with ICU patient populations or infectious disease research.Work LocationsWork will be performed in hospital intensive care units and clinical research offices. The work will be hybrid in nature - study-related tasks that are not patient-facing (screening, data capture, regulatory efforts) can be performed remotely; patient-facing activities (study recruitment, informed consent, coordination of biospecimen collection) will occur at the University of Michigan.Modes of WorkPositions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the