Cardiovascular Research Coordinator Assistant

UC Davis Health

Sacramento (CA)

In loco

USD 41.000 - 74.000

Tempo pieno

8 ore fa
Candidati tra i primi
Generatore di candidature

Distinguiti per questa posizione — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Medical plans
Dental and vision coverage
Retirement plans
CE reimbursement
Paid holidays
Paid time off
Employee assistance program

Descrizione del lavoro

UC Davis Health’s Division of Cardiovascular Medicine in Sacramento seeks an Assistant Clinical Research Coordinator to oversee multiple cardiovascular clinical trials, focusing on outpatient research. The role includes recruiting, screening, informed consent, data collection, regulatory submissions, and maintaining study binders.

Strong communication, knowledge of GCP and regulations, and willingness to travel for training are essential.

Competenze

  • Certification of laboratory safety training must be achieved on an annual basis.
  • High School graduation or sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.
  • Knowledge of Good Clinical Practices and federal, state, and university regulations for clinical research.
  • Ability to coordinate a broad range of activities from inception to implementation within strict study protocols.
  • Excellent verbal and written communication skills.

Mansioni

  • Data management and Visit Coordination.
  • Regulatory support and administration.
  • Finance and analytical support.
  • Administrative support.

Conoscenze

Clinical research
IRB submissions
Data management
Regulatory knowledge
Communication skills
GCP knowledge
Attention to detail

Formazione

Bachelor's degree in health sciences

Strumenti

Word processing software
Database software

Descrizione del lavoro

UC Davis Health’s Division of Cardiovascular Medicine in Sacramento seeks an Assistant Clinical Research Coordinator to oversee multiple cardiovascular clinical trials, focusing on outpatient research. The role includes recruiting, screening, informed consent, data collection, regulatory submissions, and maintaining study binders.

Strong communication, knowledge of GCP and regulations, and willingness to travel for training are essential.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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