Clinical Research Coordinator I

ObjectiveHealth•Folsom, CA

About The Position

ObjectiveHealth is hiring a full-time Clinical Research Coordinator to work directly with patients and conduct clinical research. The role involves taking ownership of assigned studies and patients, carrying out clinical trial protocol activities, supporting direct patient care, and maintaining accurate study data and regulatory compliance. Coordinators work with research teams, principal investigators, sponsors, monitors, and other stakeholders and may support studies in Gastroenterology, Urology, Dermatology, and/or Oncology. The successful candidate will demonstrate patient-focused care, personal responsibility, attention to detail, effective communication, and the ability to manage multiple study activities while adhering strictly to protocols and applicable regulations. ObjectiveHealth provides proprietary technology to support research-trial access, physician care options, and clinical research enrollment.

Requirements

Legal authorization to work in the United States; work visas are not currently accepted.
Strong desire to work directly with patients.
Ability to provide patient care and interact with patients.
Ability to carry out clinical trial protocol activities, including identification, screening, randomization, and enrollment.
Ability to perform or assist with patient consent, physical assessments, blood draws, medication administration, and ECGs.
Acute attention to detail and ability to maintain accurate data, regulatory compliance, and protocol adherence.
Strong communication and relationship-building skills.
Ability to stay focused while managing multiple protocols and related study activities.
Punctuality and personal responsibility.

Nice To Haves

Certification such as medical assistant (MA), phlebotomy, or similar.

Responsibilities

Conduct activities required by IRB-approved clinical trial protocols, including patient identification, screening, randomization, and enrollment.
Conduct clinic visits and perform or assist with direct patient care, including patient consent, physical assessments, blood draws, medication administration, and ECGs.
Maintain clean data entry, regulatory compliance, productive site visits, efficient study setup and maintenance, and strict protocol adherence.
Manage assigned protocols, IRB responses, audit findings, adverse event and serious adverse event tracking, and eSource materials.
Take ownership of assigned studies and patients.
Communicate promptly and effectively with leadership and coworkers about questions or issues requiring correction.
Learn and use company-provided technologies to improve day-to-day efficiency.
Ensure compliance with applicable laws, regulations, and governing-body requirements.