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

Description

Clinical Research Coordinator I

Our clinical research company is looking to hire a qualified candidate for the full‑time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.

Who We Are

ObjectiveHealth is a clinical research company that uses proprietary technology to:

1. Increase patient access to research trials within our communities,
2. Provide physicians with enhanced care options for current patients, and
3. Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.

Who You Are

• A lover of patient interaction and skilled at providing patient care
• A team player with a bias for action and an attitude that takes personal responsibility
• Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
• Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
• Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set‑up and maintenance, and strict protocol adherence
• An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
• A strong advocate for Company values, mission, and initiatives
• Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
• Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology

What Success Looks Like for This Role

• Taking ownership of assigned studies and patients
• Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
• Showing up on time, every time
• Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
• Learning and using the technologies we provide to increase efficiency in your day‑to‑day activities
• Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

What We Offer

Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short‑ and Long‑Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.