Senior CRA: CNS & Cardiovascular Trials | Regional Travel

Piper Companies

Denver (CO)

Remote

USD 100.000 - 115.000

Vollzeit

Vor 10 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Hybrid work model

Zusammenfassung

Piper Companies is seeking an experienced Senior Clinical Research Associate (CRA) to support CNS and Cardiovascular clinical studies in a sponsor-facing environment. This full-time role requires regional travel and can be located anywhere in the United States.

The CRA will oversee site performance, ensure regulatory compliance, conduct monitoring visits, SDR/SDV reviews, and maintain strong site relationships to drive trial execution and enrollment.

Qualifikationen

  • 1+ years of CRA experience, including CNS/Cardiovascular trials.
  • Strong knowledge of ICH-GCP guidelines and FDA regulations.
  • Experience with Phase II/III trials, site oversight and issue resolution.
  • Ability to conduct SIV/IMV/Closeout visits independently.
  • Strong sponsor-facing communication with biotech/pharma clients.
  • Ability to manage multiple sites and travel regionally.
  • Willingness to travel and be near a major airport.

Aufgaben

  • Monitor Phase II-III CNS and Cardiovascular trials for protocol compliance and regulatory adherence.
  • Perform site initiation, routine monitoring, and closeout visits.
  • Conduct SDR, SDV, and CRF review for data quality and inspection readiness.
  • Build partnerships with investigative sites to support enrollment and protocol adherence.
  • Provide regular updates to sponsors and study teams on site performance and progress.

Kenntnisse

Clinical Research Experience
Site management
Monitoring visits
FDA regulations
Sponsor communication

Jobbeschreibung

Piper Companies is seeking an experienced Senior Clinical Research Associate (CRA) to support CNS and Cardiovascular clinical studies in a sponsor-facing environment. This full-time role requires regional travel and can be located anywhere in the United States.

The CRA will oversee site performance, ensure regulatory compliance, conduct monitoring visits, SDR/SDV reviews, and maintain strong site relationships to drive trial execution and enrollment.

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