50 clinical research coordinator jobs at 13 companies in Romulus, MI
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Clinical Research Coordinator
Cary or Michigan or Texas or Illinois or New Jersey or North Carolina or Detroit
OnsiteFull Time
Revival Research Institute: Conducts clinical research trials to develop new medical treatments.
2+ YOERequires 2+ years coordinating industry-sponsored interventional trials at a research site, informed consent and monitoring experience, EDC proficiency, regulatory knowledge, and strong organizational and communication skills.
Electronic Data Capture (EDC), Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft Outlook, ICH-GCP, FDA, 21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 54, 21 CFR Part 56, 21 CFR Part 312, HIPAA, IATA, ECG, IRT, IWRS
Professional Case Management: Provides in-home healthcare services for patients with chronic illnesses.
Bachelor's degree or equivalent; clinical research experience preferred; ACRP/SOCRA or clinical research training preferred; proficient in Microsoft Word/Excel/PowerPoint and clinical trial databases; strong communication, organization, and regulatory knowledge.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, EDC
University of Michigan: Public research university offering undergraduate and graduate education.
2+ YOEBachelor's degree in health science or equivalent, clinical research experience, and ACRP CCRC, SOCRA CCRP, or equivalent certification. Minimum two years of directly related clinical research experience.
DM Clinical Research: A clinical research management organization providing trial services.
3+ YOEExperience as a CRC with 3+ years in coordinating industry-sponsored trials; GCP/ICH knowledge; regulatory binders; bilingual Spanish a plus; ACRP certification a plus.
GCP, ICH Guidelines, IRB, ACRP, EDC, IVRS, CRF system, Sponsor system
DM Clinical Research: Operates an integrated network of clinical trial research sites.
2+ YOEAssociates degree required; 2+ years clinical research experience and 1+ year CRC experience; LPN/CMA or pharmacy tech preferred; GCP/OSHA/IATA training; CRIO, EMR and Microsoft Office proficiency.
CRIO, Microsoft Word, Microsoft Excel, Microsoft Outlook, Google Suite
Contractor- Assistant Clinical Research Coordinator (Detroit, MI)
Detroit, Michigan, United States
OnsiteContract
Profound Research: Clinical trial network integrated into community physician practices.
3+ YOEHigh school diploma or technical degree with experience in life sciences; 1+ year with Associate’s degree; or relevant clinical/life sciences coursework/experience.
Research Study Coordinator III - Cancer Clinical & Translational Research - 40 hours - Days in Detroit, Michigan
Detroit, Michigan, United States
OnsiteFull Time
Henry Ford Health: Provides comprehensive healthcare services and health insurance in Michigan.
3+ YOECoordinate clinical research projects, ensure regulatory compliance, oversee recruitment, provide technical support to investigators; bachelor's degree and 3 years relevant experience required; SOCRA or ACRP and IATA required.
Solaris Health: National provider of specialized urological medical and surgical services.
2+ YOEMichigan RN license, BLS, accredited nursing education, bachelor's degree, and 2+ years of clinical research experience preferred; requires research coordination, data management, compliance, and patient care skills.
Electronic Data Capture (EDC), CRIO, EPIC, EHR, Envi, Microsoft Office, Microsoft Office applications, CRF, HIPAA
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Phoenix or Detroit or Boston or Charlotte or Chicago or Seattle or Cincinnati or Irving or Salt Lake City or Houston
RemoteFull Time
MedpaceNasdaq: MEDP: Full-service clinical contract research organization for medical development.
1+ YOEBachelor's in health/science, 1+ year CRC experience, valid driver's license, ability to travel 60-70% nationwide, Microsoft Office proficiency, strong communication and attention to detail.
Corewell Health: Healthcare system providing medical care and health insurance services.
3+ YOEBachelor's in nursing, active Michigan RN, CCRP or CIP with 3 years experience, BLS preferred; responsibilities include protocol coordination, enrollment, regulatory compliance, specimen handling.
Department of Veterans Affairs: Provides healthcare, benefits, and cemetery services to military veterans.
Clinical research coordination, GCP, IRB and VA research knowledge; recruitment and regulatory documentation experience; sleep apnea study experience; medical terminology knowledge; or one year of relevant study.
Good Clinical Practice (GCP), Institutional Review Board (IRB)
Alcanza Clinical Research: Operates a national network of clinical trial research sites.
1+ YOEHigh school diploma or equivalent, 1+ year clinical data entry experience, proficiency with Microsoft applications and EDC, 40+ WPM typing, knowledge of GCP/ICH/HIPAA/FDA regulations, strong communication and attention to detail.