What are the responsibilities and job description for the Clinical Research Coordinator position at Tap Growth ai?
🌟 We're Hiring: Clinical Research Coordinator! 🌟
We are seeking a detail-oriented and organized Clinical Research Coordinator to support clinical trials and research studies. The ideal candidate will have experience in clinical research operations, regulatory compliance, and patient coordination to ensure studies are conducted safely and efficiently.
📍 Location: Detroit, Michigan
What You'll Do
📝 Coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation
🤝 Interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study
🎯 Consenting new patients into clinical trials
📋 Handling lab work, including: processing lab samples, drawing blood (preferred, not required)
👥 Support with data entry and documentation
📊 Collaborate with PIs, regulatory team, and study sponsors
What We're Looking For
✅ Bachelor of Science degree
✅ Experience with Institutional Review Board (IRB) processes, including submission of new studies, renewals, and amendments.
✅ Experience in managing research study budgets, including tracking expenditures and ensuring proper allocation of funds
✅Proficient in addressing and resolving study addendums and queries from sponsors, monitors, and other research stakeholders.
Preferred Qualifications
➕ 1 –2 years of relevant experience in clinical research or healthcare setting
➕ Familiarity with medical terminology
➕ Ability To Draw Blood / Phlebotomy Skills (preferred)
➕ Detail-oriented with excellent organizational and communication skills
➕ SOCRA or ACRP and IATA certification preferred
Ready to advance medical research? 🚀 Apply now and join our mission!
We are seeking a detail-oriented and organized Clinical Research Coordinator to support clinical trials and research studies. The ideal candidate will have experience in clinical research operations, regulatory compliance, and patient coordination to ensure studies are conducted safely and efficiently.
📍 Location: Detroit, Michigan
What You'll Do
📝 Coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation
🤝 Interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study
🎯 Consenting new patients into clinical trials
📋 Handling lab work, including: processing lab samples, drawing blood (preferred, not required)
👥 Support with data entry and documentation
📊 Collaborate with PIs, regulatory team, and study sponsors
What We're Looking For
✅ Bachelor of Science degree
✅ Experience with Institutional Review Board (IRB) processes, including submission of new studies, renewals, and amendments.
✅ Experience in managing research study budgets, including tracking expenditures and ensuring proper allocation of funds
✅Proficient in addressing and resolving study addendums and queries from sponsors, monitors, and other research stakeholders.
Preferred Qualifications
➕ 1 –2 years of relevant experience in clinical research or healthcare setting
➕ Familiarity with medical terminology
➕ Ability To Draw Blood / Phlebotomy Skills (preferred)
➕ Detail-oriented with excellent organizational and communication skills
➕ SOCRA or ACRP and IATA certification preferred
Ready to advance medical research? 🚀 Apply now and join our mission!