Clinical Research Coordinator I

Socket.dev; Little Rock (AR); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

401(k) match

Health insurance

Dental insurance

Vision insurance

Paid time off

Adoption assistance

Paid holidays

Disability insurance

HSA/FSA

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I to support IRB-approved trials with direct patient care, data entry, and protocol adherence. This role emphasizes accurate documentation, patient safety, and collaboration with the study team.

The candidate will screen, enroll, and follow patients, perform basic clinical procedures, and ensure regulatory compliance across Gastroenterology, Urology, Dermatology, and Oncology studies.

Qualifications

• Clinical Research Coordinator position requires patient-care skills and IRB protocol familiarity.
• Certification such as MA, phlebotomy, or equivalent preferred.
• Ability to accurately enter data and maintain regulatory compliance.

Responsibilities

• Screen, enroll, and randomize patients for IRB-approved trials.
• Conduct clinic visits and direct patient care activities including blood draws and ECGs.
• Obtain informed consent and maintain accurate source data and eSource materials.
• Coordinate with PIs, sponsors, monitors and study team to ensure protocol adherence.

Skills

Patient care

IRB protocols

Data entry

Regulatory compliance

Team communication

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
• 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.