Clinical Research Associate - Oncology

Piper Companies; United States; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k match

Paid Holidays

Sick leave

Job summary

A leading research organization is seeking a Clinical Research Associate with direct oncology monitoring experience to work remotely with some travel. The role involves conducting site monitoring visits in accordance with GCP and ICH guidelines, overseeing regulatory submissions, and mentoring clinical staff. Ideal candidates will have 2+ years of oncology monitoring experience, strong understanding of phase 1 oncology trials, and a bachelor's degree in a related field. The compensation ranges from $90,000 to $120,000, alongside a comprehensive benefits package.

Qualifications

• 2+ years of Oncology monitoring experience required.
• Proficient in GCP and ICH guidelines.
• Able to travel locally for work.

Responsibilities

• Conduct site monitoring visits adhering to GCP and ICH guidelines.
• Collaborate with local sites to meet project needs.
• Oversee regulatory submissions and manage data queries.

Skills

Oncology monitoring experience

GCP and ICH guidelines proficiency

Onsite monitoring experience

Mentoring clinical staff

Microsoft Office and mobile devices understanding

Education

Bachelor’s degree in a related field

Job description

Piper Companies

is seeking a well‑rounded Clinical Research Associate with direct oncology monitoring experience to work with a Global CRO. The Clinical Research Associate will be working remote with some travel included.

Requirements

• 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

• 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 (phase 2 and 3 are welcomed)
• Bachelor’s degree in a related field

Compensation

• 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

This job opens for applications on 12/4/2025. Applications for this job will be accepted for at least 30 days from the posting date.