RN Clinical Research Coordinator for CNS Trials

CenExel

Decatur (GA)

Sur place

USD 55 000 - 75 000

Plein temps

Il y a 5 jours
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Avantages offerts par ce poste

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STD
Life Ins
401k

Résumé du poste

CenExel is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials in line with ICH, GCP, and sponsor guidelines. The role emphasizes patient engagement, data integrity, and regulatory compliance across trials in a fast-paced environment.

Responsibilities include organizing trial information, observing participants, data analysis, data collection, and reporting. A Georgia RN license is required, with CCRC preferred; travel may be involved.

Qualifications

  • Must have mastery of Clinical Research Coordinator I responsibilities.
  • Georgia RN license required; CCRC certification preferred.
  • 2-3 years of medical field experience recommended.
  • Knowledge of Federal regulations protecting human subjects in research.

Responsabilités

  • Coordinate patient involvement for studies from initiation to completion.
  • Organize research information for trials.
  • Observe subjects and assist with data analysis and reporting.
  • Schedule data collection and ensure quality and compliance.
  • Report adverse events and protocol deviations as appropriate.
  • Assist CTM with vendor oversight, training, and staff development.

Connaissances

Clinical coordination
Regulatory knowledge
Communication skills
Team leadership
Problem solving

Formation

Georgia RN license
CCRC certification preferred

Description du poste

CenExel is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials in line with ICH, GCP, and sponsor guidelines. The role emphasizes patient engagement, data integrity, and regulatory compliance across trials in a fast-paced environment.

Responsibilities include organizing trial information, observing participants, data analysis, data collection, and reporting. A Georgia RN license is required, with CCRC preferred; travel may be involved.

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