ObjectiveHealth

AI-powered in-practice clinical trial platform

Clinical Research Coordinator 2

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeSt. Louis, MO, USANo salary listedIn-person

About the Job

Requirements

At least 3 years of clinical research coordination experience.
Legal authorization to work in the United States is required.
The candidate must be skilled in all aspects of conducting an Institutional Review Board-approved clinical trial protocol, including patient identification, screening, randomization, enrollment, and clinic visits.
The candidate must be skilled in direct patient care activities, including obtaining patient consent, physical assessments, blood draws, medication administration, and electrocardiograms.
The candidate must maintain accurate data entry, regulatory compliance, productive site visits, efficient study setup and maintenance, and strict protocol adherence.
The candidate must manage multiple protocols, resolve and submit Institutional Review Board responses and audit findings, track adverse event and serious adverse event events, and maintain electronic source material for assigned studies.

Responsibilities

Take ownership of assigned studies and patients.
Conduct clinical trial activities, including patient identification, screening, randomization, enrollment, and clinic visits.
Perform and assist with direct patient care activities, including patient consent, physical assessments, blood draws, medication administration, and electrocardiograms.
Maintain accurate study data, regulatory compliance, study setup and maintenance, and protocol adherence.
Resolve and submit Institutional Review Board responses and audit findings.
Track adverse event and serious adverse event events and maintain electronic source material for assigned studies.
Communicate promptly and effectively with leadership and coworkers when questions arise or corrections are needed.
Use provided technologies to increase efficiency in daily activities.
Ensure compliance with applicable laws, regulations, and governing-body requirements.

Desired Qualifications

Experience in clinical research involving gastroenterology, urology, dermatology, and/or oncology.

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:

Increase patient access to research trials within our communities,
Provide physicians with enhanced care options for current patients, and
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.

About the Company

ObjectiveHealth

AI-powered in-practice clinical trial platform

Objective Health integrates clinical research into everyday care by partnering with physician practices, community health centers, and health systems to run on-site study teams and manage trials. Its platform uses ObjectiveScreen to analyze electronic health records and pre-qualify patients, while ObjectiveView gives sponsors a transparent view of trial progress and data. The model includes on-site staffing and end-to-end study management to speed recruitment and improve data quality. Its goal is to broaden access to clinical trials through local, partner-based research and to expand across therapeutic areas.

Company size: 51-200
Company stage: Growth Equity (Venture Capital)
Total funding: $23.6M
Headquarters: Franklin, TN
Founded: 2018

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