Clinical Research Associate - Oncology

  • ZP Group Expired
  • Vancouver, Washington
  • Full Time

This job ad was removed 1 day ago.

Job Description


Piper Companies is seeking a well-rounded Clinical Research Associate with direct oncology monitoring experience. The Clinical Research Associate will be working remote with some travel included.

Requirements for the Clinical Research Associate include:

  • Conducting site monitoring visits in line with GCP and ICH guidelines
  • Ensure project needs are met by collaborating with local sites
  • Oversee regulatory submissions, CRF completion, and data query resolutions
  • Ensure documentation is properly formatted and filed; TMF and ISF
  • Mentor clinical staff during visits

Qualifications for the Clinical Research Associate include:

  • 2+ years of Oncology monitoring experience
  • 2+ years of onsite monitoring experience
  • Able to travel locally for work
  • Proficient in GCP and ICH guidelines
  • Understand Microsoft Office and mobiles devices
  • Strong understanding of Phase 1 oncology trials
  • Bachelor's degree in a related field

Compensation for the Clinical Research Associate includes:

  • Salary range: $90,000 - $120,000
  • Comprehensive benefit package: Medical, Dental, Vision, 401k match plus PTO, Sick leave as required by law, and Paid Holidays

Keywords: Clinical research associate, CRA, hospital, travel, oncology, documentation, trials, trial sites, cancer, cancer research, GCP, ICH, recruitment plans, projects, project, protocol adherence, regulatory submissions, enrollment, CRF completion, data, data query, start-up phase, phase 1, trial master file, TMF, Investigators site file, ISF, mentorship, Microsoft office, mobile devices

#LI-BH1 #LI-REMOTE

This job opens for applications on 5/16/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Piper Companies is seeking a well-rounded Clinical Research Associate with direct oncology monitoring experience. The Clinical Research Associate will be working remote with some travel included.

Requirements for the Clinical Research Associate include:

  • Conducting site monitoring visits in line with GCP and ICH guidelines
  • Ensure project needs are met by collaborating with local sites
  • Oversee regulatory submissions, CRF completion, and data query resolutions
  • Ensure documentation is properly formatted and filed; TMF and ISF
  • Mentor clinical staff during visits

Qualifications for the Clinical Research Associate include:

  • 2+ years of Oncology monitoring experience
  • 2+ years of onsite monitoring experience
  • Able to travel locally for work
  • Proficient in GCP and ICH guidelines
  • Understand Microsoft Office and mobiles devices
  • Strong understanding of Phase 1 oncology trials
  • Bachelor's degree in a related field

Compensation for the Clinical Research Associate includes:

  • Salary range: $90,000 - $120,000
  • Comprehensive benefit package: Medical, Dental, Vision, 401k match plus PTO, Sick leave as required by law, and Paid Holidays

Keywords: Clinical research associate, CRA, hospital, travel, oncology, documentation, trials, trial sites, cancer, cancer research, GCP, ICH, recruitment plans, projects, project, protocol adherence, regulatory submissions, enrollment, CRF completion, data, data query, start-up phase, phase 1, trial master file, TMF, Investigators site file, ISF, mentorship, Microsoft office, mobile devices

#LI-BH1 #LI-REMOTE

This job opens for applications on 5/16/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Job ID: 478416291
Originally Posted on: 5/25/2025

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