Clinical Research Nurse

We are looking for a Clinical Research Nurse with prior clinical research experience in a hospital or clinical setting. We are open to candidates seeking temp to hire.
Schedule: Monday- Friday (very little evenings or weekends unless requested) 8-4:30 or 9-5 (30 min lunch)
The Clinical Research Nurse will perform nursing assessments and procedures, such as conducting comprehensive nursing assessments, obtain vital signs, review medications, document patient information/instructions in the medical record, complete appropriate forms. Perform any procedures required for the patient such as drawing blood, conducting EKG's etc. Collect and interpret clinical and research information related to the patient visit. Appropriately field/triage patient telephone calls regarding medication changes, clinical status, prescription renewals, or changes in condition.
Phase depends on trail. Will either be phase 2, 3 or 4
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy:
Required Skills & Experience
Must Haves: PA Nursing License, BLS from AHA or ARC
Clinical Research Experience: At least 2 years of experience in clinical research within a hospital or academic setting (experience from industry settings is not applicable).
Phlebotomy Skills: Ability to draw blood.
Injection Skills: Ability to perform injections.
Primary Responsibilities:
Participant Coordination: Coordinate the recruitment and enrollment of research participants.
Database Management: Establish and maintain databases of subjects.
Study Visits: Schedule and conduct study visits.
Data Collection and Entry: Collect and enter data; register subjects and study visits in OnCore.
Billing Review: Perform Epic research billing review.
Regulatory Compliance: Maintain an up-to-date regulatory binder.
Sponsor Visits: Schedule and attend sponsor visits.
IRB Compliance: Prepare and submit IRB paperwork to ensure compliance with IRB regulations.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.