Clinical Research Technician/Assistant

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　　Summary

　　The Judith Tam ALK Lung Cancer Research Initiative is a new initiative in the Rogel Cancer Center focused on accelerating progress in discoveries related to the pathogenesis, progression, treatment, and prevention of ALK driven lung cancers. The overarching purpose of this initiative is to foster rapid adoption of key discoveries that directly enhance the quality and length of the life of patients.

　　In this position, you will join a multidisciplinary team focused on researching ALK+ lung cancers of patients presenting at the University of Michigan as well as partnering institutions. The ideal candidate would have exceptional interpersonal skills, timely execution, and attention to detail. This self-starter would be responsible for helping coordinate the clinical research efforts to fulfill the mission and vision of the ALK Initiative.

　　This position may independently provide study coordination for simple and moderately complex clinical research studies. As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity. Mastery of all job duties from the CRC-Assistant position on theMichigan Medicine CRC Career Ladder (https://research.medicine.umich.edu/our-units/clinical-trials-support-office/clinical-research-coordinator-career-ladder) is required.

　　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:

　　Characteristic Duties and 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

　　Responsibilities will include, but are not limited to:

　　Work with the present study team to coordinate and execute sponsor and/or investigator-initiated clinical trials. These activities include, but are not limited to: screening, consenting, patient communication, data abstraction and entry, attending clinical team and research related meetings, and maintaining required research certifications.

　　Achieve in-depth understanding of study protocols and objectives to assist with successful implementation of all study procedures.

　　Perform screening and coordinate recruitment efforts with various key stakeholders to obtain specimens from both U-M and partnering institutions. This includes making potential participant phone calls and accompanying them to the procedure room or blood draw. Attending tumor board if needed and research related meetings will also be required.

　　Conduct direct and professional interaction with study participants in a clinical, phone, or virtual setting and act as a liaison between patients, investigators, and laboratory team.

　　Assist with tissue/sample procurement, transport, patient interaction, patient on-boarding, and sample preparation for multi-omic analysis.

　　Assist with the accurate input and management of patient research data in an organized and timely manner. Responsibilities may include:

　　OnCore patient and clinical study registration and data management

　　Create, code, and manage REDCap database housing for clinical data samples

　　Conduct data modeling exercises using REDCap, statistical software including SPSS, GraphPad Prism, Tableau

　　Create, model, and update genomic sample database with multiple clinical/sequencing/drug testing overlapping variables.

　　Assist with creating study/research related documents, graphics, and presentations for Initiative-wide use.

　　Presentation of clinical team recruitment, data, and study status at ALK team meetings.

　　Assist with miscellaneous tasks as required by research group including ALK website upkeep.

　　Supervision Received: This position receives direct supervision and reports directly to the ALK Program Manager and Principal Investigator.

　　Supervision Exercised: None.

　　Required Qualifications*

　　Clinical Research Technician:

　　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 area 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.

　　It is imperative in this position to be a pro-active team member and be willing to assist other team members as needed.

　　Excellent writing skills.

　　Excellent and timely communication skills.

　　The ability to manage multiple ongoing projects and meet multiple deadlines.

　　The ability to work independently, demonstrate outstanding organizational skills and judgment.

　　The ability to collaborate with a diverse team.

　　The flexibility, reliability, and time management skills required to fulfill and perform job duties both in person and remotely.]

　　Clinical Research Assistant:

　　High school diploma or GED is necessary.Desired Qualifications*

　　Clinical Research Technician:

　　Bachelor 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.

　　Clinical Research Assistant:

　　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

　　Full-time, working weekdays both in person and remote with the need for flexibility for occasional evening hours and the rare weekend. Part-time may be considered for the right applicant.

　　Underfill Statement

　　This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.

　　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

　　244296

　　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-Hematology/Oncology

　　Posting Begin/End Date

　　1/22/2024 - 2/05/2024

　　Career Interest

　　Research

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