Remote CRA II for Cardiovascular & CNS Trials

Piper Companies

United States

Remote

USD 100,000 - 125,000

Full time

12 days ago

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Job summary

Piper Companies is seeking a Clinical Research Associate II for a remote permanent role with 60-75% travel across the United States. The CRA II will support cardiovascular, CNS, and metabolic studies while partnering with investigative sites to ensure high-quality trial execution.

Requirements include 1–4 years of onsite monitoring experience and a life sciences degree. Travel-heavy position offers a competitive salary and comprehensive benefits package in a global clinical research setting.

Qualifications

  • 1–4 years of onsite clinical monitoring experience.
  • Experience supporting trials in cardiovascular, CNS, diabetes or metabolic indications.
  • Strong knowledge of GCP, ICH, and FDA regulatory requirements.
  • Proficiency with CTMS, EDC, and standard clinical trial documentation.

Responsibilities

  • Perform routine and close-out monitoring visits to ensure studies comply with GCP, ICH and regulations.
  • Serve as primary contact for assigned sites and maintain strong communications.
  • Review site data, source documents, and regulatory files for accuracy and protocol adherence.
  • Provide guidance and training to site staff on protocol requirements and procedures.
  • Identify and document quality or compliance concerns and support resolutions.

Skills

GCP knowledge
Site monitoring
Regulatory compliance
Site coordination

Education

Bachelor’s degree in life sciences or related field

Tools

CTMS
EDC

Job description

Piper Companies is seeking a Clinical Research Associate II for a remote permanent role with 60-75% travel across the United States. The CRA II will support cardiovascular, CNS, and metabolic studies while partnering with investigative sites to ensure high-quality trial execution.

Requirements include 1–4 years of onsite monitoring experience and a life sciences degree. Travel-heavy position offers a competitive salary and comprehensive benefits package in a global clinical research setting.

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