Clinical Research Coordinator II

ObjectiveGI, Inc.; Columbia Township (MO); Sur place; USD 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

401(k) with company match

Health Savings Account & Flexible StIP

Health, Dental and Vision insurance

Generous PTO

Adoption Assistance

Paid Holidays

Résumé du poste

ObjectiveHealth is seeking a Clinical Research Coordinator II in Missouri to support multiple GI, urology, dermatology and oncology trials. You will manage patient consent, scheduling and data entry, ensuring protocol adherence and regulatory compliance in a fast-paced clinical setting.

The role emphasizes accurate documentation, collaboration with PIs, sponsors and monitors, and delivering high-quality enrollment metrics across diverse studies.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience with IRB approved protocols and regulatory requirements.
• Strong patient interaction and data-entry accuracy.

Responsabilités

• Identify, screen, randomize and enroll patients per protocol.
• Conduct clinic visits and direct patient care activities (consenting, assessments, blood draws, ECG).
• Maintain regulatory compliance and clean data entry across the study.

Connaissances

Clinical research coordination

Description du poste

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.