Clinical Research CMA: IP Dispensing & Coordinator

Dm Clinical Research Group

Phoenix (AZ)

Vor Ort

USD 42.000 - 54.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

DM Clinical Research Group is seeking a Certified Medical Assistant to join as an Unblinded Clinical Research Coordinator in Phoenix, AZ. The role involves dispensing Investigational Products (IP) and coordinating clinical trial activities alongside the Principal Investigator and sponsor.

The candidate will measure vital signs, collect specimens, administer injections, and ensure IP accountability and regulatory compliance across study sites.

Qualifikationen

  • Associates Degree required or 2 years of formal educational coursework.
  • Bachelor's degree, preferred.
  • Secondary or Foreign Medical Graduate, preferred.

Aufgaben

  • Dispense Investigational Products (IP) per protocol.
  • Measure vital signs and document medical histories.
  • Collect blood and other specimens for testing.
  • Administer injections or vaccines and monitor adverse reactions.
  • Interact with PI, sponsor, study manager and coordinators to ensure protocol compliance.
  • Maintain IP accountability and proper storage of IP and samples.
  • Ensure regulatory documents and site certifications are up to date.

Kenntnisse

Communication skills
Customer service
Time management
Bilingual Spanish

Ausbildung

Associate's Degree
Bachelor's degree preferred
Foreign/Secondary Medical Graduate
2 years coursework

Tools

CRIO
Microsoft Word
Excel
Google Suite

Jobbeschreibung

DM Clinical Research Group is seeking a Certified Medical Assistant to join as an Unblinded Clinical Research Coordinator in Phoenix, AZ. The role involves dispensing Investigational Products (IP) and coordinating clinical trial activities alongside the Principal Investigator and sponsor.

The candidate will measure vital signs, collect specimens, administer injections, and ensure IP accountability and regulatory compliance across study sites.

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