Clinical Research Coordinator: Drive Patient-Centric Trials

ELEVATE CLINICAL RESEARCH, INC.

Santee (CA)

In loco

USD 34.000 - 48.000

Tempo pieno

7 ore fa
Candidati tra i primi

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Descrizione del lavoro

Elevate Clinical Research, Inc. is seeking a Clinical Research Coordinator to manage trial activities within healthcare settings, coordinating patient recruitment, informed consent, scheduling visits, and data capture while ensuring regulatory compliance and Good Clinical Practice.

This role interfaces with investigators, study sponsors, and clinical teams to ensure data integrity, participant safety, and timely study progress, contributing to impactful research nationwide.

Competenze

  • Bachelor's degree in a health-related field.
  • At least 2 years of clinical research coordination experience.
  • Knowledge of regulatory requirements and GCP guidelines.
  • Experience with informed consent forms and case report forms.
  • Strong organizational and communication skills.

Mansioni

  • Coordinate day-to-day clinical trial operations including recruitment, consent, and scheduling visits.
  • Ensure regulatory compliance, GCP adherence, and timely documentation.
  • Maintain regulatory documents, case report forms, and study databases.
  • Monitor participant safety and report adverse events as required.
  • Collaborate with investigators, sponsors, and study teams to resolve issues.

Conoscenze

Clinical trial coordination
Regulatory documentation
Informed consent forms
Data management

Formazione

Bachelor's degree in a health-related field

Strumenti

EDC systems
CTMS

Descrizione del lavoro

Elevate Clinical Research, Inc. is seeking a Clinical Research Coordinator to manage trial activities within healthcare settings, coordinating patient recruitment, informed consent, scheduling visits, and data capture while ensuring regulatory compliance and Good Clinical Practice.

This role interfaces with investigators, study sponsors, and clinical teams to ensure data integrity, participant safety, and timely study progress, contributing to impactful research nationwide.

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