Research Senior Supervisor

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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.

The University of Michigan Cardiometabolic Research Center is a newly established, first-of-its-kind research center with PI's Dr. Ambarish Pandey and Dr. Thomas Wang. The Center's mission is to optimize cardiometabolic health and reduce cardiovascular risk across the health system through a data science-driven, risk-based approach spanning six integrated cores:
Population and Data Science, Phenotyping, Cardiometabolic Health Clinic and Clinical Trials, Health System Implementation, Industry and Academic Partnerships, and Training and Education. The Research Senior Supervisor will serve as the operational backbone of this multidisciplinary clinical research enterprise, providing administrative and scientific coordination across active clinical trials, observational studies, and translational research initiatives. This individual will report directly to the co-PIs of the Cardiometabolic Center, support a group of 15-20 personnel, and will play a central role in building and sustaining the research infrastructure of the Center from the ground up.

• Oversee day-to-day operations of the Cardiometabolic Center research program, including coordination of active clinical trials, observational cohort studies, and translational research projects across all Center cores.
• Manage IRB submissions, regulatory documentation, and clinical trial compliance in accordance with federal regulations, institutional policies, and sponsor requirements (GCP/ICH).
• Supervise, mentor, and coordinate research coordinators, data analysts, and other research staff; lead hiring, onboarding, and performance evaluation processes.
• Coordinate multi-site research activities and serve as the primary liaison with external collaborators, industry partners, and academic institutions participating in Center studies.
• Develop and implement standard operating procedures (SOPs) for research operations, data management, quality assurance, and participant safety monitoring.
• Support grant development and reporting activities, including preparation of NIH and industry-sponsored progress reports, budget tracking, and regulatory submissions.
• Oversee research data management and integrity across platforms including REDCap, EPIC, and other clinical data systems used by the Center.
• Facilitate the recruitment, screening, consent, and enrollment of research participants across Center studies in collaboration with the clinical trials team.
• Coordinate internal and external communications for the Center, including preparation of presentations, manuscripts, newsletters, and reports for stakeholders and funding agencies.
• Monitor Center finances, manage procurement, and assist in budget planning, tracking, and reconciliation across funded projects.

• Education:
  
  Masters degree in Clinical Research, Public Health, Biomedical Sciences, Epidemiology, or a related field.
• Experience:
  
  Minimum 3-5 years of experience in clinical research coordination or program management, including direct experience with IRB protocols, clinical trial operations, and research compliance.
• Skills:
  
  Exceptional organizational, written, and interpersonal communication skills; demonstrated ability to manage multiple concurrent projects in a complex, multidisciplinary research environment.
• Technical Knowledge:
  Proficiency with research management platforms (REDCap, EPIC, or equivalent); familiarity with GCP/ICH guidelines and clinical trial regulatory requirements.
• Compliance:
  Demonstrated knowledge of research ethics, human subjects protection, and institutional compliance requirements for federally funded and industry-sponsored clinical research.

• PhD in Clinical Research, Public Health, Biomedical Sciences, Epidemiology, or a related field.
• Experience:
  
  5+ years of clinical research program management, including demonstrated leadership of multi-site clinical trials or federally funded cardiovascular or cardiometabolic research programs.
• Familiarity with cardiometabolic diseases, heart failure, or cardiovascular clinical research
• Experience with data science tools, EHR-based research platforms, and large clinical datasets.
• Prior grant management or sponsored research administration experience, including NIH and/or industry-funded clinical trials.