Clinical Research Coordinator II

ObjectiveHealth•Wells Township, MI

19d

About The Position

ObjectiveHealth is hiring a full-time Clinical Research Coordinator II to conduct and coordinate clinical research trials. The role involves working directly with patients, managing assigned studies, supporting patient care, maintaining study documentation and data, and ensuring compliance with approved protocols and applicable regulations. Research areas may include Gastroenterology, Urology, Dermatology, and/or Oncology. The successful candidate takes ownership of assigned studies and patients, communicates effectively with leadership and coworkers, learns and uses company-provided technologies, and embodies the company values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication. The position requires legal authorization to work in the United States; work visas are not currently accepted.

Requirements

At least 3 years of clinical research coordination experience.
Strong interest and skill in patient interaction and patient care.
Experience with the activities required to conduct an IRB-approved clinical trial protocol.
Ability to perform or assist with patient care activities such as consenting, physical assessments, blood draws, medication administration, and ECGs.
Attention to detail in data entry, regulatory compliance, study visits, study setup and maintenance, and protocol adherence.
Strong communication and relationship-building skills.
Ability to stay focused while managing multiple protocols and related study tasks.
Legal authorization to work in the United States; work visas are not currently accepted.

Nice To Haves

Interest in clinical research in Gastroenterology, Urology, Dermatology, and/or Oncology.

Responsibilities

Conduct IRB-approved clinical trial activities, including patient identification, screening, randomization, enrollment, and clinic visits.
Perform or assist with direct patient care, including informed consent, physical assessments, blood draws, medication administration, and ECGs.
Maintain accurate data entry, regulatory compliance, study setup and maintenance, and adherence to study protocols.
Communicate and foster relationships among the research team, principal investigators, sponsors, monitors, leadership, and coworkers.
Manage multiple protocols; prepare and submit IRB responses; address audit findings; track adverse events (AEs) and serious adverse events (SAEs); and maintain eSource material for assigned studies.
Take ownership of assigned studies and patients and communicate promptly 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.