Clinical Research Associate, Oncology

Proven Recruiting; San Diego (CA); On-site; USD 52,000 - 92,000; Full time

Job summary

Proven Recruiting is seeking a Clinical Research Associate to support Phase 2 oncology trials in San Diego, CA. You will monitor sites, ensure protocol and regulatory compliance, and collaborate with investigators and staff to optimize enrollment and data quality.

Requirements include a Life Sciences-related bachelor’s degree and 4+ years of clinical research, with oncology experience preferred. Travel up to 30% is expected; compensation ranges from $38.00 to $67.00 per hour.

Qualifications

• 4+ years of clinical research experience.
• Oncology clinical trial experience strongly preferred.
• Knowledge of ICH/GCP guidelines, FDA regulations, HIPAA.
• Ability to travel up to 30% for site monitoring visits.

Responsibilities

• Conduct site qualification, initiation, monitoring, and closeout visits while ensuring compliance with study protocols, SOPs, and regulatory requirements.
• Review source documentation and CRF data, resolve queries, monitor protocol deviations, and ensure timely SAE reporting and study deliverables.
• Partner with investigators and site staff to provide training, support enrollment efforts, maintain essential documents and eTMF records, and drive overall site performance.

Skills

Clinical research experience

ICH GCP

FDA regulations

HIPAA

Travel willingness

Education

Bachelor’s degree in Life Sciences or related field

Job description

Clinical Research Associate - San Diego, CA - $38.00 - $67.00/hour

Looking for a Clinical Research Associate opportunity where you can contribute to cutting-edge oncology programs and make a meaningful impact on patient care? Our client, an innovative clinical-stage biotech company, is seeking a motivated CRA to support Phase 2 clinical trials while working alongside a collaborative and mission-driven clinical operations team.

Who you are:

• Bachelor’s degree in Life Sciences, Nursing, or a related field.
• 4+ years of clinical research or healthcare industry experience, including 3+ years of direct field monitoring experience.
• Oncology clinical trial experience strongly preferred.
• Strong knowledge of ICH/GCP guidelines, FDA regulations, HIPAA, and the drug development process.
• Ability to travel up to 30% for site monitoring visits.

What you’ll do:

• Conduct site qualification, initiation, monitoring, and closeout visits while ensuring compliance with study protocols, SOPs, and regulatory requirements.
• Review source documentation and CRF data, resolve queries, monitor protocol deviations, and ensure timely SAE reporting and study deliverables.
• Partner with investigators and site staff to provide training, support enrollment efforts, maintain essential documents and eTMF records, and drive overall site performance.

What does this position pay?

Compensation is determined by several factors which may include skillset, experience level, and education.

The expected range for this role is $38.00 - $67.00 per hour. Please note this range is an estimate and actual pay may vary based on qualifications and experience.

We actively support and promote people of various backgrounds, from race, religion, gender to geographical area, university, lifestyle, and personality type. Proven Recruiting is minority-owned, majority women, and is a strong advocate for diversity and inclusion in the broader community.