Clinical Research Coordinator I: Data & Visits

Dm Clinical Research Group

Phoenix (AZ)

Vor Ort

USD 52.000 - 75.000

Vollzeit

14 Tage+
Bewerbungsgenerator

Schick keinen Standard-Lebenslauf — erstelle einen Lebenslauf und ein Anschreiben, die genau auf diese Rolle zugeschnitten sind.

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Benefits dieser Stelle

None

Zusammenfassung

DM Clinical Research Group in Phoenix, AZ is seeking a Clinical Research Coordinator I to join our site and ensure high-quality data collection in line with sponsor protocols, FDA regulations, and ICH/GCP guidelines. You will help enrollment meet sponsor expectations and support timely company goals.

Responsibilities include completing required trainings, conducting visits, maintaining ALCOA-C records, data entry, and coordinating with staff, investigators and sponsors to facilitate smooth study

Qualifikationen

  • 1+ years as a CRC, preferably coordinating industry-sponsored vaccines in private settings.
  • 2+ years as a research assistant, data coordinator, or lab personnel in clinical research.
  • ACRP certification preferred; Registered Medical Assistant preferred.

Aufgaben

  • Complete all required training on a timely basis (ICH-GCP, IATA, protocol, EDC/IVRS).
  • Conduct subject visits and document procedures per protocol and ALCOA-C standards.
  • Enter data and resolve queries per guidelines and sponsor expectations.
  • Liaise with laboratory, data, admin, investigators, staff and sponsor representatives.
  • Assist with subject recruitment and retention and obtain informed consent.

Kenntnisse

Detail-oriented
Multitasking
Communication skills
Bilingual English/Spanish

Ausbildung

High School Diploma
Bachelor's degree
Foreign Medical Graduates preferred

Jobbeschreibung

DM Clinical Research Group in Phoenix, AZ is seeking a Clinical Research Coordinator I to join our site and ensure high-quality data collection in line with sponsor protocols, FDA regulations, and ICH/GCP guidelines. You will help enrollment meet sponsor expectations and support timely company goals.

Responsibilities include completing required trainings, conducting visits, maintaining ALCOA-C records, data entry, and coordinating with staff, investigators and sponsors to facilitate smooth study

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