Piper Companies
Clinical Research Associate - Oncology
Piper Companies, Lansing, Michigan, United States, 48900
Piper Companies
We are 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 .
Responsibilities
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 mobile 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, protocol adherence, regulatory submissions, enrollment, CRF completion, data query, phase 1, trial master file, TMF, Investigators site file, ISF, mentorship, Microsoft office, mobile devices
Application Information This job opens for applications on 12/12/2025. Applications for this job will be accepted for at least 30 days from the posting date.
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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 .
Responsibilities
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 mobile 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, protocol adherence, regulatory submissions, enrollment, CRF completion, data query, phase 1, trial master file, TMF, Investigators site file, ISF, mentorship, Microsoft office, mobile devices
Application Information This job opens for applications on 12/12/2025. Applications for this job will be accepted for at least 30 days from the posting date.
#J-18808-Ljbffr