CRA home based Florida

Resourcing Life Science Ltd.

Florida

Presencial

USD 70.000 - 90.000

Jornada completa

14 días+

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Descripción de la vacante

Resourcing Life Science is seeking a Senior Clinical Research Associate (CRA) to work from home in Florida. In this role, you will monitor clinical studies in phases II-III, ensuring adherence to Good Clinical Practices and supervising study conduct according to required regulations.

The ideal candidate holds a Bachelor degree in life-science and has at least 1 to 5 years of experience in monitoring. Excellent communication and fluent English skills are essential.

Formación

  • Min 1/5 year monitoring experience as CRA / Clinical Research Associate within a CRO, Pharma, Biotech.
  • Experience in commercial studies.
  • Experience with site initiation and close out.
  • Experience in clinical studies phase II-III.

Responsabilidades

  • Monitoring clinical studies in phases II-III.
  • Assuring adherence to Good Clinical Practices and compliance with study procedures.
  • Supervising study conduct according to GCP requirements.

Conocimientos

Monitoring clinical studies
Communication skills
Fluent English

Educación

Bachelor degree in life-science

Descripción del empleo

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a senior CRA / Clinical Research Associate Home Based in Florida.

Job Overview
  • Monitoring clinical studies in phases II-III
  • Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
  • Identification, qualification and initiation of investigators and their sites.
  • Supervising study conduct according to GCP requirements and all applicable laws.
Key Requirements
  • Bachelor degree in life-science
  • Min 1/5 year monitoring experience as CRA / Clinical Research Associate within a CRO, Pharma, Biotech
  • Experience in commercial studies
  • Experience with site initiation, site close out
  • Experience in clinical studies phase II-III
  • Fluent English
  • Excellent communication skills
  • A full clean drivers license
  • FTE: 1.0
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