Sr. Contract Clinical Research Associate (Oncology)
Piper Companies · United States
- Hybrid
- Contract
- $135,200 / year
- United States
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Sr. Contract Clinical Research Associate (Oncology)
Piper Companies · United States
Riley Chen
Hiring Manager · h•••••@careers.pipercompanies.com
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Subject: Interested in the Sr. Contract Clinical Research Associate (Oncology) role at Piper Companies
Hi Riley — I came across the Sr. Contract Clinical Research Associate (Oncology) opening and wanted to reach out directly. I've spent the last few years doing exactly this kind of work, and Piper Companies stood out because…
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Not recommended alone — most applicants never hear back.
Job highlights
- Remote contract role for Oncology CRA.
- Requires 5+ years CRA, 3+ oncology experience.
- Monitor sites, ensure compliance, verify data.
- Travel 8-10 days/month across US regions.
- Competitive hourly rate with full benefits.
About the role
Sr. Contract Clinical Research Associate (Oncology)
Piper Companies is seeking a Sr. Contract Clinical Research Associate (Oncology) to support oncology clinical trials within the pharmaceutical and biotechnology industry. The Sr. Contract Clinical Research Associate (Oncology) role is ideal for an experienced CRA with strong oncology monitoring experience and the ability to travel across multiple U.S. regions. The Sr. Contract Clinical Research Associate (Oncology) role is a remote opportunity that requires you to travel 8-10 days per month for onsite monitoring and is a contract opportunity.
Responsibilities
- Conduct site initiation, monitoring, and close-out visits for oncology studies.
- Ensure compliance with protocols, ICH-GCP, SOPs, and regulatory requirements.
- Verify source data, CRFs, and EDC entries for accuracy and completeness.
- Identify and document protocol deviations and safety issues.
- Prepare timely monitoring reports and maintain trial documentation.
Requirements
- 5+ years of CRA experience within pharmaceutical, biotechnology, or CRO settings.
- 3+ years of strong oncology clinical trial monitoring experience.
- Solid understanding of ICH-GCP and FDA regulations.
- Ability to independently manage multiple sites.
- Willingness to travel 8–10 days per month across PST, CST, and MST.
Compensation
- $55.00 - $65.00 per hour (Depending on Experience)
- Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
Key skills/competency
- Clinical Research Associate
- Oncology Clinical Trials
- Clinical Monitoring
- ICH-GCP
- CRO
- Pharmaceutical
- Biotechnology
- Site Management
- Regulatory Compliance
- Data Verification
Skills & topics
- Clinical Research Associate
- Oncology
- Clinical Trials
- CRA
- ICH-GCP
- Biotechnology
- Pharmaceutical
- Remote
- Contract
- Monitoring
How to get hired
- Tailor your resume: Highlight your 5+ years of CRA experience and 3+ years of oncology clinical trial monitoring. Emphasize your understanding of ICH-GCP and FDA regulations.
- Showcase site management skills: Detail your ability to independently manage multiple sites and conduct all types of site visits (initiation, monitoring, close-out).
- Quantify achievements: Use data to demonstrate your success in ensuring compliance, verifying data accuracy, and identifying/documenting deviations.
- Prepare for travel: Be ready to discuss your willingness and ability to travel 8-10 days per month across PST, CST, and MST time zones.
- Express your interest: Clearly state your enthusiasm for supporting oncology clinical trials and your fit for a contract, remote role.
Technical preparation
Master ICH-GCP and FDA regulations.,Practice site initiation/monitoring protocols.,Review oncology trial case studies.,Familiarize yourself with EDC systems.
Behavioral questions
Describe a challenging site you managed.,How do you ensure data accuracy?,How do you handle protocol deviations?,How do you manage competing site priorities?
Prefer to apply the usual way?
Not recommended alone — most applicants never hear back. Email the hiring manager first.
Frequently asked questions
- What is the work arrangement for the Sr. Contract Clinical Research Associate (Oncology) role at Piper Companies?
- The Sr. Contract Clinical Research Associate (Oncology) position at Piper Companies is a remote role. While you will work remotely, it requires travel 8-10 days per month for onsite monitoring visits across multiple U.S. regions.
- What are the key experience requirements for the Sr. Contract Clinical Research Associate (Oncology) position?
- To be considered for the Sr. Contract Clinical Research Associate (Oncology) role, you need at least 5 years of overall CRA experience and a minimum of 3 years specifically in oncology clinical trial monitoring. A strong understanding of ICH-GCP and FDA regulations is also essential.
- What is the compensation for the Sr. Contract Clinical Research Associate (Oncology) role?
- The Sr. Contract Clinical Research Associate (Oncology) role offers an hourly rate between $55.00 and $65.00, depending on your experience. Additionally, a full comprehensive benefits package is provided.
- What is the expected travel for the Sr. Contract Clinical Research Associate (Oncology) position?
- As a Sr. Contract Clinical Research Associate (Oncology), you can expect to travel approximately 8-10 days per month. This travel is required for conducting onsite monitoring visits across the PST, CST, and MST regions of the United States.
- What therapeutic area is the Sr. Contract Clinical Research Associate (Oncology) focused on?
- The Sr. Contract Clinical Research Associate (Oncology) position is specifically focused on supporting oncology clinical trials. Strong experience in oncology monitoring is a key requirement for this role.