Clinical Research Coordinator I — Direct Patient Care

ObjectiveHealth; Columbia Township (MO); Sur place; USD 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

401(k) with Company match

Health, Dental and Vision insurance

PTO and Holidays

Disability insurance

HSA/FSA

Career advancement pathway

Adoption assistance

Résumé du poste

ObjectiveHealth is seeking a Clinical Research Coordinator I to join as a full-time team member. The successful candidate will have MA or phlebotomy certification and enjoy hands-on patient care, coordinating IRB-approved trials, and coordinating with physicians and sponsors.

The role requires safe patient interaction, accurate data entry, strict regulatory compliance, and timely communication with the research team.

Qualifications

• Certification such as MA or phlebotomy required.
• Experience conducting IRB-approved clinical trial protocols (identification, screening, randomization, enrollment).
• Ability to consent patients, perform blood draws, ECG, and other direct patient care activities.
• Strong attention to data entry, regulatory compliance, and audit readiness.
• Excellent communication and collaboration with study teams and sponsors.

Responsabilités

• Own assigned studies and patients.
• Communicate with leadership and coworkers about issues or corrections.
• Maintain punctuality and reliability in daily activities.

Connaissances

Patient interaction

Team player

IRB protocol experience

Direct patient care

Data accuracy

Regulatory compliance

Communication

Formation

MA certification

Phlebotomy certification

Outils

eSource systems

Electronic data capture

Description du poste

ObjectiveHealth is seeking a Clinical Research Coordinator I to join as a full-time team member. The successful candidate will have MA or phlebotomy certification and enjoy hands-on patient care, coordinating IRB-approved trials, and coordinating with physicians and sponsors.

The role requires safe patient interaction, accurate data entry, strict regulatory compliance, and timely communication with the research team.