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Clinical Research Associate

Piper Companies

Louisiana

Remote

USD 90,000 - 120,000

Full time

Yesterday
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Job summary

A global leader in clinical research is seeking a Clinical Research Associate for a remote position. The CRA will monitor clinical trials, ensuring compliance with guidelines and managing communication with study sites. Ideal candidates will have oncology monitoring experience and a relevant degree. This role offers a competitive salary and comprehensive benefits.

Benefits

Medical (Cigna)
Dental (Guardian)
Vision (VSP)
401K (Voya through ADP)

Qualifications

  • At least 2 years of onsite oncology monitoring experience.
  • Strong therapeutic and protocol knowledge in Phase 1 oncology trials.

Responsibilities

  • Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines.
  • Track study progress, including regulatory approvals, enrollment, data collection, and query resolution.

Skills

Oncology Monitoring
GCP
ICH Guidelines
Patient Recruitment
Protocol Knowledge

Education

Bachelor's degree in life sciences
Advanced degree preferred

Tools

CTMS
EDC
Microsoft Office Suite

Job description

Join to apply for the Clinical Research Associate role at Piper Companies.

1 day ago Be among the first 25 applicants.

Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote position. The CRA will monitor and participate in clinical trials across the country for a leading Clinical Research Organization.

Responsibilities of the Clinical Research Associate include:
  • Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines.
  • Support subject recruitment and adapt recruitment plans as needed.
  • Provide protocol training and manage communication with study sites.
  • Assess site adherence to protocol and regulatory requirements, reporting quality issues.
  • Track study progress, including regulatory approvals, enrollment, data collection, and query resolution.
  • Maintain accurate site documentation, including visit reports and regulatory files.
Qualifications for the Clinical Research Associate include:
  • At least 2 years of onsite oncology monitoring experience.
  • Proficiency in CTMS, EDC, and Microsoft Office Suite.
  • Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Experience in site management, patient recruitment, and clinical trial documentation.
  • Strong therapeutic and protocol knowledge in Phase 1 oncology trials.
  • Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred).
Compensation for the Clinical Research Associate:
  • Salary Range: $90,000-$120,000 (USD).
  • Comprehensive Benefits: Medical (Cigna), Dental (Guardian), Vision (VSP), sick leave if required by law, and 401K (Voya through ADP).
Additional Details:

This job opens for applications on 4/21 and will be accepting applications for at least 30 days from the posting date.

Job Details:
  • Seniority level: Entry level.
  • Employment type: Full-time.
  • Job function: Research, Analyst, and Information Technology.
  • Industries: Business Consulting and Services.

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