Senior Oncology Clinical Research Associate (Remote)

TRIO - Translational Research in Oncology; Dallas (TX); Remote; USD 110,000 - 132,000; Full time

Benefits offered by this job

Health benefits for you and family (TR

Vacation time

Personal/sick time

401(k) with employer matching

Home office allowance

Internet allowance

Luggage allowance

Flexible working hours

Job summary

TRIO - Translational Research in Oncology is seeking a Senior Clinical Research Associate (CRA) to join our Monitoring Resources team. This is a full-time, remote position for candidates based in the Central and Western United States and will require travel to clinical trial sites.

Responsibilities include site visits, ensuring FDA/ICH-GCP compliance, managing regulatory documents, data verification, and mentoring junior CRAs.

Qualifications

• Minimum 5 years oncology experience as CRA/CRC/Research Nurse.
• Minimum 2 years monitoring on early phase trials.
• Phase I trial monitoring experience preferred.
• Experience in solid tumor trials (breast, lung, gastric, ovarian, pancreatic).
• Fluent in English; science-related Bachelor's degree.
• Strong ICH-GCP knowledge and trial processes.
• Experience with clinical trial information systems.

Responsibilities

• Conduct site visits (pre-study to termination).
• Ensure FDA/ICH-GCP compliance and regulatory document completion.
• Perform data verification of source documents.
• Ensure FDA/ICH-GCP guideline adherence.
• Assist with budget negotiations and follow-up where applicable.
• Mentor junior CRAs on-site.

Skills

Oncology CRA experience

Monitoring experience

Phase I monitoring

Solid tumor trials

Fluent English

Bachelor's degree

ICH-GCP knowledge

Clinical trial systems

Travel readiness

Mentoring

Education

Science-related Bachelor's degree

Tools

CTMS

Job description

TRIO - Translational Research in Oncology is seeking a Senior Clinical Research Associate (CRA) to join our Monitoring Resources team. This is a full-time, remote position for candidates based in the Central and Western United States and will require travel to clinical trial sites.

Responsibilities include site visits, ensuring FDA/ICH-GCP compliance, managing regulatory documents, data verification, and mentoring junior CRAs.