Clinical Research Coordinator Associate

Full Time Mid Level 2+ years

Posted 1 week ago

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About This Role

Join a fast-growing obstetrics research team to support clinical trials and manage multiple projects aimed at maternal and neonatal health outcomes. This role involves assisting investigators, coordinating patient recruitment, and ensuring compliance with study protocols.

Responsibilities

  • Assist multiple investigators and collaborators to monitor patient recruitment and develop plans to enhance recruitment
  • Coordinate with the interprofessional team at the Partnering for the Future Clinic and community referral organizations
  • Screen, recruit, approach and consent pregnant women, giving study overview while being sensitive to environment and patients involved
  • Attain in-depth understanding of study protocol and objectives to assist with successful implementation of all study procedures
  • Execute study visits and study related procedures
  • Collect human biospecimens, process, prepare, and ship specimens to outside institutions according to study protocol requirements
  • Submit Human Subjects Incentive Program (HSIP) requests
  • Create case report forms, questionnaires and study related documents
  • Complete study documentation in various data systems
  • Assist PI and study team in maintaining IRB (eResearch) applications including scheduled continuing reviews, adverse event reporting, and other reportable information

Requirements

  • Bachelor's degree or equivalent
  • Certification as CCRC or CCRP (or obtained within six months of hire)
  • 2+ years of experience in clinical research and clinical trials

Qualifications

  • Bachelor's degree or an equivalent combination of related education and experience
  • Minimum 2 years of directly related experience in clinical research and clinical trials

Nice to Have

  • 4+ years of direct related experience
  • At least 1 year of experience working with patients with OUD/SUD
  • Doula certified
  • Experience with OnCore clinical trial management system (CTMS)
  • Previous experience with MiChart, RedCap, or Qualtrics
  • At least 1 year of experience working with maternal populations or reproductive health
  • Previous experience with chart abstraction and/or data entry

Skills

Qualtrics * REDCap * MiChart * GCPs * OnCore * IRB *

* Required skills

Certifications

Certified Clinical Research Coordinator (CCRC) (Required) Certified Clinical Research Professionals (CCRP) (Required)

About University of Michigan

Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development.

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