Clinical Research Coordinator I

ObjectiveGI, Inc.; Akron, Northern (OH, KY); Hybrid; USD 48,000 - 62,000; Full time

Benefits offered by this job

Competitive compensation

401(k) with Company match

Career advancement pathway

Disability insurance

HSA & FSA

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I to join our team in the United States. The role focuses on direct patient interaction, accurate data entry, and strict adherence to IRB-approved protocols while coordinating multiple studies.

You will perform patient screenings, consent processes, and study visits, ensuring regulatory compliance and high-quality data. A passion for patient care and teamwork will help drive enrollment and trial success across Gastroenterology, Urology,

Qualifications

• Certification such as MA or phlebotomy.
• Experience conducting IRB approved clinical trial protocols.
• Ability to consent patients, perform phlebotomy, ECG and other patient care tasks.
• Strong data entry and regulatory compliance focus.

Responsibilities

• Take ownership of assigned studies and patients.
• Communicate promptly with leadership and coworkers when questions arise or corrections are needed.
• Maintain punctuality and reliability in daily activities.
• Ensure strict regulatory compliance with governing bodies and study protocols.
• Learn and use provided technologies to increase day-to-day efficiency.
• Uphold company values of Compassion, Integrity, Collaboration, Innovation, Velocity and Dedication.

Skills

Patient interaction

Data entry

Regulatory compliance

Communication skills

Attention to detail

Study coordination

IRB protocol

Job 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.