Job Information
University of Michigan Clinical Research Technician/Assistant in Ann Arbor, Michigan
Clinical Research Technician/Assistant
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Summary
The Pulmonary Hypertension Research Team consists of three physicians, two nurse practitioners, four nurses and three research coordinators dedicated to working toward a common goal of providing the best possible care for patients with pulmonary hypertension. The teams' shared commitment to excellence, strong work ethic, and sense of unity results in high-quality research. The team primarily focuses on industry sponsored novel clinical drug trials, but also participates in PI initiated studies and registries. The PH Research Team is looking for a highly motivated, detail oriented, individual with a passion for research and patient care to join the team.
Mission Statement
Michigan 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.
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 1850. Michigan Medicine is comprised of over 30,000 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 savings
Responsibilities*
Experience as part of a team with all 8 competency domains is expected:
Scientific Concepts and Research Design
Ethical Participant Safety Considerations
Investigational Products Development and Regulation
Clinical Study Operations (GCPs)
Study and Site Management
Data Management and Informatics
Leadership and Professionalism
Communication and Teamwork
In this role you will be responsible for but not limited to the following: (Please note this is not a laboratory tech position, and job duties do not include performing laboratory assays)
Liaise with the present Study Coordinators to coordinate and execute sponsor and/or investigator-initiated clinical trials.
Attain in-depth understanding of study protocols and objectives to assist with successful implementation of all study procedures. Coordinate recruitment of patients for pulmonary hypertension trials and patient education relative to study participation.
Perform medical chart review, patient screening, informed consent processes, scheduling and conducting patient clinic visits, data processing, and diagnostic and therapeutic interventions.
Directly interact with study patients in a clinical setting, act as liaison between patients, investigators, nurses, other departments, sponsors, vendors, and regulatory agencies.
Manage patient research data accurately in an organized and timely manner; adverse event reporting; prepare appropriate reports for investigators and/or sponsors including maintaining and completing the supplied case report forms; project reports as required by study sponsors.
Coordination and participation in site visits with the sponsor/CRO. Manage and coordinate data related to patient participation in studies, workflow as needed by multiple studies, and participate in maintaining regulatory files.
This position requires excellent written and oral communication skills. To be successful in this position the self-motivated candidate should have a working knowledge of Good Clinical Practice (GCP), as well as governmental and local regulations governing clinical research.
The candidate must possess strong interpersonal skills with exceptional attention to detail and critical thinking skills. Candidates must be able to meet multiple concurrent deadlines independently. The candidate must demonstrate project management ability and a positive approach and capacity to accept feedback and use it to improve individual and team performance. It is imperative in this position to be a pro-active team member and be willing to assist other team members as needed.
Supervision Received: This position receives direct supervision and reports directly to the programs lead CRC and Faculty Principal Investigator.
Supervision Exercised: None.
Required Qualifications*
Technician Level:
Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRAs Definition of a Clinical Research Professional for qualifying experience prior to applying.) or An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD. or Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
Candidate must possess IT proficiency in Microsoft Word, PowerPoint, Excel, Outlook, and Adobe office products
Assistant Level:
- High school diploma or GED is necessary.
Desired Qualifications*
Technician Level:
Bachelor's degree in Health Science or an equivalent combination of related education and experience is desirable.
An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures
Certifications through ACRP or SoCRA are preferred but not required. Experience in scheduling appointments (in a clinical or non-clinical setting), using eResearch, EPIC (MiChart) and OnCore.
Previous experience scheduling, and project management.
Assistant Level:
- Associate Degree in Health Science or an equivalent combination of related education and experience is desirable. An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.
Work Schedule
Hours: 40/week
Shift: Onsite Monday-Friday 8a-4:30p
Underfill Statement
This position may be underfilled at the CRC-Assistant title based on selected candidates' qualifications.
Additional Information
Michigan Medicine is firmly committed to advancing inclusion, diversity, equity, accessibility, and belonging, which are core to the culture and values of the Medical School Office of Research. Our community supports recruiting and cultivating a diverse workforce as a reflection of our commitment to serve the diverse people of Michigan and the world. We strive to create a work culture where each team member feels respected, valued, and safe.
Background Screening
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.
Application Deadline
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.
U-M EEO/AA Statement
The University of Michigan is an equal opportunity/affirmative action employer.
Job Detail
Job Opening ID
249358
Working Title
Clinical Research Technician/Assistant
Job Title
Clinical Research Technician
Work Location
Ann Arbor Campus
Ann Arbor, MI
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Int Med-Cardiology
Posting Begin/End Date
6/11/2024 - 6/25/2024
Career Interest
Research
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