Clinical Research Coordinator: Drive Protocols & Data

Community Health Network; Indianapolis, Northern (IN, KY); Hybrid; USD 52,000 - 64,000; Full time

Job summary

Community Health Network in Indianapolis, IN seeks a Clinical Research Coordinator to assess, plan, implement and execute protocol-driven studies with the Principal Investigator and team. The role requires obtaining informed consent, maintaining data management systems, collecting data, preparing case report forms, and coordinating with sponsors and sites while upholding GCP, ICH and regulatory standards.

This full-time position offers opportunities to lead study activities, collaborate across

Qualifications

• Associate degree required; bachelor’s degree preferred.
• CCRA/CCRC/CCRP certifications within 3 years of hire.
• Minimum 2 years of related healthcare experience.
• Experience with data abstraction is helpful.
• Ability to obtain informed consent and manage data.

Responsibilities

• Identify and screen eligible candidates for study eligibility.
• Obtain informed consent from eligible patients for a study.
• Maintain an effective data management system to track participants and activities.
• Collect data and complete case report forms and data queries as specified by protocol.
• Prepare source documents for data collection.
• Assist in identifying study-related procedures for the project budget.
• Attend Investigator and Coordinator meetings and sponsor visits.
• Perform phlebotomy and ECG testing as trained.
• Process laboratory specimens for shipment per protocol; report results.
• Coordinate, implement and ensure compliance with GCP/ICH and regulatory standards.

Skills

Phlebotomy

ECG

Data collection

Source documentation

Communication

Education

Associate degree

Bachelor's degree

Job description

Community Health Network in Indianapolis, IN seeks a Clinical Research Coordinator to assess, plan, implement and execute protocol-driven studies with the Principal Investigator and team. The role requires obtaining informed consent, maintaining data management systems, collecting data, preparing case report forms, and coordinating with sponsors and sites while upholding GCP, ICH and regulatory standards.

This full-time position offers opportunities to lead study activities, collaborate across