Remote Oncology CRA | Senior CRA (Contract)

Translational Research in Oncology

United States

Remoto

USD 90.000 - 130.000

Tempo pieno

7 giorni fa
Candidati tra i primi
Generatore di candidature

Trasforma questo annuncio in un colloquio — un curriculum e una lettera di presentazione creati in base a ciò questo datore di lavoro sta cercando.

Supera i filtri ATS

Descrizione del lavoro

Translational Research in Oncology (TRIO) is seeking an experienced Clinical Research Associate (CRA) or Senior CRA to join the Monitoring Resources team. This is a remote independent contractor role, full-time for one year, with applicants based in the United States and preference for Central or Western regions.

Responsibilities include data verification, performing site visits (pre-study to termination), and ensuring compliance with FDA/ICH-GCP guidelines.

Competenze

  • 3+ years as CRA/monitoring in oncology trials.
  • 1+ year monitoring on early-phase trials.
  • Experience with solid tumor trials preferred.

Mansioni

  • Perform data verification of source documents.
  • Conduct site visits from pre-study to termination.
  • Ensure adherence to FDA, ICH-GCP and local regulations.
  • Ensure implementation and compliance with FDA, and ICH-GCP guidelines.
  • Assist with data validation and query resolution.
  • Mentor junior team members as required.
  • Ensure completion and collection of regulatory documents.

Conoscenze

Oncology experience
English fluency
Regulatory knowledge
Travel willingness

Formazione

Bachelor's degree in science

Strumenti

Clinical trial systems

Descrizione del lavoro

Translational Research in Oncology (TRIO) is seeking an experienced Clinical Research Associate (CRA) or Senior CRA to join the Monitoring Resources team. This is a remote independent contractor role, full-time for one year, with applicants based in the United States and preference for Central or Western regions.

Responsibilities include data verification, performing site visits (pre-study to termination), and ensuring compliance with FDA/ICH-GCP guidelines.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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