Senior CNS & Rare Disease CRA — Remote Midwest Travel

Worldwide Clinical Trials

Kansas

Remoto

USD 97.000 - 193.000

Tempo pieno

5 giorni 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

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to ensure high-quality, compliant studies from site qualification through closeout.

You will partner with investigative sites, study teams, and sponsors, lead monitoring visits, train site personnel, and support data quality and safety across the lifecycle.

This home-based role covers the Midwest, requires 8–10 travel days per month, and offers a competitive benefits package with transparent compensation.

Competenze

  • Bachelor's Degree or a Nursing Degree, along with 5+ years as a regional, traveling Clinical Research Associate.
  • Required experience monitoring CNS and Rare Disease clinical trials.
  • Requires travel within the specified region; 8 – 10 DOS monthly.
  • Experience in full-service monitoring preferred.
  • Strong knowledge of clinical trial processes, site management, and regulatory requirement

Mansioni

  • Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
  • Identify and assess potential research sites to support successful study execution.
  • Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
  • Conduct all types of monitoring visits: PSSVs, SIVs, IMVs and COVs.
  • Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
  • Monitor site performance and provide ongoing support throughout study maintenance activities.
  • Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
  • Partner with sites and study teams to drive data quality, participant safety, and overall study success.
  • Support site closeout activities and ensure study requirements are completed at the conclusion of the trial.

Conoscenze

Regional traveling CRA
CNS & Rare Disease monitoring
Full-service monitoring
Regulatory knowledge

Formazione

Bachelor's Degree
Nursing Degree

Descrizione del lavoro

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to ensure high-quality, compliant studies from site qualification through closeout.

You will partner with investigative sites, study teams, and sponsors, lead monitoring visits, train site personnel, and support data quality and safety across the lifecycle.

This home-based role covers the Midwest, requires 8–10 travel days per month, and offers a competitive benefits package with transparent compensation.

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