Senior Clinical Research Associate – Global Trials Lead

ProTrials Research, Inc.

United States

Vor Ort

USD 95.000 - 150.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

ProTrials Research, Inc. is seeking a Contract Senior Clinical Research Associate to join our team. The Sr.

CRA plays an integral part in the successful monitoring and management of clinical trials, ensuring studies are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH GCP, and all applicable regulatory requirements. Travel up to 65% may be required. The role involves training sites, managing data quality, regulatory documentation, and maintaining strong communication

Qualifikationen

  • Detail-oriented and organized with strong interpersonal communication.
  • Excellent organizational and problem-solving skills.
  • Flexible travel up to 65% and ability to manage multiple sites.

Aufgaben

  • Monitor clinical studies and site visits across stages (qualification, initiation, interim, close-out).
  • Train site personnel on protocol requirements and source data.
  • Manage investigational supplies, dispensing, inventory, and reconciliation.
  • Review data, CRFs, and regulatory documentation for accuracy and compliance.
  • Maintain study files and regular contact with investigators, coordinators, and client personnel.
  • Support CRA I/II and provide solutions to project teams.

Kenntnisse

Detail-oriented
Organizational skills
Interpersonal skills
Problem solving
Travel flexibility
MS Office

Ausbildung

RN or Bachelor's in biological sciences

Tools

FDA regulations

Jobbeschreibung

ProTrials Research, Inc. is seeking a Contract Senior Clinical Research Associate to join our team. The Sr.

CRA plays an integral part in the successful monitoring and management of clinical trials, ensuring studies are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH GCP, and all applicable regulatory requirements. Travel up to 65% may be required. The role involves training sites, managing data quality, regulatory documentation, and maintaining strong communication

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