Onsite Oncology Data Coordinator (Part-Time)

ACTalent; Philadelphia (Philadelphia County); On-site; USD 34,000 - 45,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Disability insurance (short/long-term)

Health Spending Account (HSA)

Paid time off

Job summary

ACTalent is hiring a Part Time Clinical Research Coordinator (Oncology) in Philadelphia, PA. This onsite role focuses on accurate data capture, timely query resolution, and clear communication with patients and site staff. The position is 24 hours per week.

Responsibilities include data entry, chart review, query resolution, and ensuring GCP/compliance. Prior oncology trial experience and HIPAA/GCP training are preferred.

Qualifications

• Experience as a Clinical Research Coordinator.
• At least 2 years of experience with electronic data capture data entry.
• Hands-on experience working on oncology clinical trials.
• Proficiency with electronic data capture systems and electronic medical records (EMR).
• Training in HIPAA and Good Clinical Practice (GCP).

Responsibilities

• Collect and enter clinical trial data accurately and promptly into electronic data capture systems.
• Review source documents and patient charts to ensure data completeness and protocol compliance.
• Identify, investigate, and resolve data queries in trial data systems.
• Communicate clearly with patients and site staff about the clinical trial.
• Collaborate with the site research team to maintain protocol and regulatory compliance.
• Maintain meticulous records to support monitoring visits and audits.
• Prioritize tasks to meet study timelines and data entry deadlines.
• Work onsite in a professional clinical setting with clinical and research staff.

Skills

Clinical Research Coord

EDC data entry

Oncology trials

EMR software

HIPAA training

GCP training

Data accuracy

Communication

Tools

EMR

EDC

Job description

ACTalent is hiring a Part Time Clinical Research Coordinator (Oncology) in Philadelphia, PA. This onsite role focuses on accurate data capture, timely query resolution, and clear communication with patients and site staff. The position is 24 hours per week.

Responsibilities include data entry, chart review, query resolution, and ensuring GCP/compliance. Prior oncology trial experience and HIPAA/GCP training are preferred.