Clinical Research Coordinator I — Patient-Focused Trials

ObjectiveHealth; Akron (OH); On-site; USD 45,000 - 60,000; Full time

Benefits offered by this job

401(k) with company match

Health, Dental and Vision insurance

Paid time off

Adoption assistance

Paid holidays

Job summary

ObjectiveHealth is a clinical research company that focuses on increasing patient access to trials and delivering robust enrollment metrics for sponsors. A Clinical Research Coordinator I will work directly with patients, screen and enroll participants, and perform clinic visits including phlebotomy and ECG.

The role emphasizes strong data integrity, regulatory compliance, and collaboration with investigators to advance trials in gastroenterology, urology, dermatology, and oncology.

Qualifications

• IRB-approved clinical trial protocol execution: identification, screening, randomization, and enrollment of patients

Responsibilities

• Consent patients and conduct clinic visits, including blood draws and ECGs
• Ensure accurate data entry and regulatory compliance across trials
• Support site visits, protocol adherence and enrollment metrics

Skills

Patient care

IRB protocol execution

Clinical data entry

Regulatory compliance

Communication

Tools

ECG equipment

Blood draw equipment

Job description

ObjectiveHealth is a clinical research company that focuses on increasing patient access to trials and delivering robust enrollment metrics for sponsors. A Clinical Research Coordinator I will work directly with patients, screen and enroll participants, and perform clinic visits including phlebotomy and ECG.

The role emphasizes strong data integrity, regulatory compliance, and collaboration with investigators to advance trials in gastroenterology, urology, dermatology, and oncology.