Michigan Medicine
Clinical Research Coord Assoc. TERM LIMITED
Michigan Medicine, Ann Arbor, Michigan, us, 48113
Clinical Research Coord Assoc. TERM LIMITED
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Clinical Research Coord Assoc. TERM LIMITED
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Michigan Medicine
Job Summary The Judith Tam ALK Lung Cancer Research Initiative in the Rogel Cancer Center Department of Internal Medicine Division of Hematology/Oncology is a team science, collaborative program to advance precision medicine for patients with ALK+ NSCLC. Through the creation of a diverse multidisciplinary team and broad collaborations, we focus on accelerating 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 life of patients.
Role Overview 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 globally. You will serve as the lead coordinator for a large longitudinal registry that is being established. The ideal candidate has in-depth experience with AI, registry-based research, and biostatistics, along with exceptional interpersonal skills, timely execution, and high attention to detail.
Term 2‑year term‑limited position, possible renewal for additional year(s) based on funding and performance.
Responsibilities
Oversee study startup, database management, screening, consenting, patient communication, data abstraction and entry, research meetings, and regulatory management tasks.
Understand study protocols and objectives to assist with successful implementation of all study procedures.
Develop best research practices for a large active registry study.
Coordinate recruitment efforts and obtain specimens from U‑M and partner institutions.
Interact professionally with study patients via clinical, virtual, and phone settings and act as liaison between patients, database tech support, investigators, and laboratory team.
Assist with tissue/sample procurement, transport, onboarding, and preparation for multi‑omic analysis.
Maintain accurate patient research data in an organized and timely manner (OnCore registration, REDCap or other registry database).
Conduct data modeling exercises using REDCap, SPSS, GraphPad Prism, Tableau.
Create and update genomic sample database and statistical reports.
Coordinate research activities across faculty, laboratory staff, and research staff; manage meeting coordination.
Assist with study documents, graphics, presentations, and publications.
Present clinical team recruitment, data, and study status at ALK team and advisory board meetings.
Required Qualifications
Bachelor’s degree in Health Science or equivalent combination of education and experience.
Certified Clinical Research Coordinator (CCRC) by ACRP or Certified Clinical Research Professional (CCRP) by SOCRA; certification must be obtained within six months of hire.
Minimum 2 years of directly related experience in clinical research and trials.
Knowledge and experience in biostatistics.
Proficient in working with AI.
Desired Qualifications
4+ years of experience.
Bachelor’s in Scientific Nursing with clinical research experience.
Experience with large registry studies.
Experience with AI EMR integration.
Data science certification.
CITI Human Subjects and GCP certification.
Work Schedule On-site, full-time. Requires flexibility for early mornings, evenings, occasional travel, and rare weekend work. 80% position may be considered.
Modes of Work Positions may be eligible for hybrid or mobile/remote work at discretion of the hiring department.
Additional Information This is a 2-year term-limited appointment. At the end of the stated term, the appointment will terminate and will not be eligible for Reduction-in-Force benefits.
Background Screening Michigan Medicine conducts background screening and pre-employment drug testing on candidates upon acceptance of a contingent job offer.
Application Deadline Job postings are open for at least seven calendar days. The review and selection process may begin at the eighth day. The opening may be removed from posting boards and filled after the minimum posting period.
U‑M EEO Statement The University of Michigan is an equal employment opportunity employer.
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Clinical Research Coord Assoc. TERM LIMITED
role at
Michigan Medicine
Job Summary The Judith Tam ALK Lung Cancer Research Initiative in the Rogel Cancer Center Department of Internal Medicine Division of Hematology/Oncology is a team science, collaborative program to advance precision medicine for patients with ALK+ NSCLC. Through the creation of a diverse multidisciplinary team and broad collaborations, we focus on accelerating 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 life of patients.
Role Overview 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 globally. You will serve as the lead coordinator for a large longitudinal registry that is being established. The ideal candidate has in-depth experience with AI, registry-based research, and biostatistics, along with exceptional interpersonal skills, timely execution, and high attention to detail.
Term 2‑year term‑limited position, possible renewal for additional year(s) based on funding and performance.
Responsibilities
Oversee study startup, database management, screening, consenting, patient communication, data abstraction and entry, research meetings, and regulatory management tasks.
Understand study protocols and objectives to assist with successful implementation of all study procedures.
Develop best research practices for a large active registry study.
Coordinate recruitment efforts and obtain specimens from U‑M and partner institutions.
Interact professionally with study patients via clinical, virtual, and phone settings and act as liaison between patients, database tech support, investigators, and laboratory team.
Assist with tissue/sample procurement, transport, onboarding, and preparation for multi‑omic analysis.
Maintain accurate patient research data in an organized and timely manner (OnCore registration, REDCap or other registry database).
Conduct data modeling exercises using REDCap, SPSS, GraphPad Prism, Tableau.
Create and update genomic sample database and statistical reports.
Coordinate research activities across faculty, laboratory staff, and research staff; manage meeting coordination.
Assist with study documents, graphics, presentations, and publications.
Present clinical team recruitment, data, and study status at ALK team and advisory board meetings.
Required Qualifications
Bachelor’s degree in Health Science or equivalent combination of education and experience.
Certified Clinical Research Coordinator (CCRC) by ACRP or Certified Clinical Research Professional (CCRP) by SOCRA; certification must be obtained within six months of hire.
Minimum 2 years of directly related experience in clinical research and trials.
Knowledge and experience in biostatistics.
Proficient in working with AI.
Desired Qualifications
4+ years of experience.
Bachelor’s in Scientific Nursing with clinical research experience.
Experience with large registry studies.
Experience with AI EMR integration.
Data science certification.
CITI Human Subjects and GCP certification.
Work Schedule On-site, full-time. Requires flexibility for early mornings, evenings, occasional travel, and rare weekend work. 80% position may be considered.
Modes of Work Positions may be eligible for hybrid or mobile/remote work at discretion of the hiring department.
Additional Information This is a 2-year term-limited appointment. At the end of the stated term, the appointment will terminate and will not be eligible for Reduction-in-Force benefits.
Background Screening Michigan Medicine conducts background screening and pre-employment drug testing on candidates upon acceptance of a contingent job offer.
Application Deadline Job postings are open for at least seven calendar days. The review and selection process may begin at the eighth day. The opening may be removed from posting boards and filled after the minimum posting period.
U‑M EEO Statement The University of Michigan is an equal employment opportunity employer.
#J-18808-Ljbffr