Part-Time Cardiology Research Coordinator

Actalent; Las Vegas (NV); On-site; USD 34,000 - 48,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Health Savings Account (HSA)

Short and long-term disability

Life Insurance

PTO/Vacation

Job summary

Actalent is seeking a part-time Clinical Research Coordinator to support a cardiology clinical trial in Las Vegas, NV. The role involves data integrity, patient engagement, and adherence to regulatory requirements with approximately 20 hours per week and onsite duties.

Responsibilities include data entry into EDC, eligibility verification via EMR, and collaboration with investigators to ensure protocol timelines are met. HIPAA and GCP training are expected.

Qualifications

• Minimum 1+ years of experience with electronic data capture (EDC).
• Experience with electronic medical records (EMR).
• Hands-on clinical research in a trial setting.

Responsibilities

• Serve as one of the primary Clinical Research Coordinators for an ongoing cardiology clinical trial.
• Manage multiple study activities independently with high accuracy and organization.
• Enter data timely and accurately into EDC systems and resolve data queries.

Skills

Clinical Research Coordinator

EDC data entry

EMR experience

HIPAA training

GCP training

Independent worker

Data integrity

Participant engagement

Communication skills

Job description

Actalent is seeking a part-time Clinical Research Coordinator to support a cardiology clinical trial in Las Vegas, NV. The role involves data integrity, patient engagement, and adherence to regulatory requirements with approximately 20 hours per week and onsite duties.

Responsibilities include data entry into EDC, eligibility verification via EMR, and collaboration with investigators to ensure protocol timelines are met. HIPAA and GCP training are expected.