Patient-Focused Clinical Research Coordinator I

Objective; South Bend (IN); On-site; USD 52,000 - 75,000; Full time

Benefits offered by this job

401(k) match

Health, Dental and Vision insurance

Generous PTO

Job summary

ObjectiveHealth seeks a Clinical Research Coordinator I to support IRB‑approved trials across Gastroenterology, Urology, Dermatology and Oncology. The ideal candidate will have MA or phlebotomy certification and enjoy direct patient contact, helping move studies from screening through enrollment with accuracy and compassion.

You will work with the research team to conduct clinic visits, obtain patient consent, perform basic procedures (blood draws, ECG), maintain eSource data, and ensure

Qualifications

• Certification such as MA or phlebotomy required or preferred.
• Experience in conducting IRB approved clinical trial protocols.
• Ability to perform patient consent, basic clinical procedures, and data entry.

Responsibilities

• Screen and enroll patients for clinical trials.
• Conduct clinic visits and basic procedures (blood draws, ECG).
• Ensure regulatory compliance and accurate data entry.

Skills

Patient interaction

Attention to detail

Regulatory compliance

Communication

Team collaboration

Education

MA or phlebotomy certification

Tools

ECG

eSource data entry

IRB protocols

Job description

ObjectiveHealth seeks a Clinical Research Coordinator I to support IRB‑approved trials across Gastroenterology, Urology, Dermatology and Oncology. The ideal candidate will have MA or phlebotomy certification and enjoy direct patient contact, helping move studies from screening through enrollment with accuracy and compassion.

You will work with the research team to conduct clinic visits, obtain patient consent, perform basic procedures (blood draws, ECG), maintain eSource data, and ensure