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Master’s degree (or foreign equivalent) in Molecular Biology, Cellular Biology, Biomedical Sciences, Pharmacology, or a related field, and one (1) year of experience
Job Code Number
Job Description
Coordinate and support clinical trials across start-up, conduct, and close-out; prepare and submit IRB/IEC applications and amendments; maintain study master files and documentation in compliance with ICH-GCP and applicable regulations; track timelines, enrollment, and visit schedules; oversee data collection and query resolution in EDC/CRFs and assist with PK/PD sample tracking and vendor communications; monitor safety reporting workflows (AEs/SAEs) to ensure timely notifications; liaise with Principal Investigators, research sites, and cross-functional teams to ensure protocol adherence and data quality; assist with development of study tools (source documents, checklists) and prepare periodic status reports for management and stakeholders.
Additional Requirements
Mail resume to SciTech Development, Inc., 281 Kercheval Ave, Grosse Pointe Farms, MI 48236.
Scitech Development, Inc
Employer Website
Grosse Pointe Farms, Michigan 48236
364932121
1
4/3/2026
11-9121.01
Clinical Research Coordinators
Masters Degree or above
