Clinical Research Coordinator II

ObjectiveHealth; Columbia Township (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) plan

Health, Dental, Vision

Paid time off

Adoption assistance

FSA benefits

Job summary

ObjectiveHealth in the United States seeks a Clinical Research Coordinator II to join our patient-centered team. You will coordinate IRB-approved protocols, screen and enroll patients, and manage patient visits while ensuring accurate data collection.

The ideal candidate has 3+ years of clinical research coordination experience, strong communication, and a diligent eye for detail to support investigators, sponsors, and monitors, upholding regulatory compliance and patient safety.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience with IRB approved protocols.
• Experience with patient consenting, visits, and data collection.

Responsibilities

• Own assigned studies and patient visits.
• Coordinate screening, enrollment, and follow-up per protocol.
• Ensure regulatory compliance and accurate data entry.
• Collaborate with investigators, sponsors, monitors.

Job description

Description

Clinical Research Coordinator II

Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal candidate will possess 3+ years of clinical research coordination experience, 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.