Clinical Research Coordinator II — Patient Care & Trials

ObjectiveHealth; St. Louis (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) with match

Health, Dental, Vision

Paid Time Off

Disability insurance

HSA/FSA

Paid Holidays

Adoption Assistance

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our patient-focused team. This full-time role requires 3+ years of clinical research coordination experience and a passion for working directly with patients in IRB-approved trials.

You will manage study activities, screen and enroll participants, perform visits, consent patients, and ensure data quality and regulatory compliance. A collaborative, patient-centric mindset and strong communication with investigators, sponsors,

Qualifications

• Experience with IRB-approved trial protocols.
• Experience obtaining informed consent and conducting patient care activities.
• Strong data entry and regulatory compliance.
• Experience in GI/Urinary/Urology/Oncology trials is a plus.

Responsibilities

• Own assigned studies and patients; ensure timely progress.
• Communicate promptly with leadership and coworkers when corrections are needed.
• Maintain punctuality and reliability in all duties.
• Ensure compliance with all governing laws and regulations.
• Learn and use provided technologies to increase day-to-day efficiency.
• Uphold Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication.

Skills

Patient interaction

Team player

Attention to detail

Communication

Protocol adherence

Data entry

IRB protocols

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our patient-focused team. This full-time role requires 3+ years of clinical research coordination experience and a passion for working directly with patients in IRB-approved trials.

You will manage study activities, screen and enroll participants, perform visits, consent patients, and ensure data quality and regulatory compliance. A collaborative, patient-centric mindset and strong communication with investigators, sponsors,