Join Us! We gave an position available at our Eye Care Special located in beautiful Kingston, PA. As an experiences Licensed Practical Nurse (Clinical Research Coordinator), You'll join a team of innovative and accomplished providers, surgeons, and clinical care staff.

We offer an excellent salary with production based bonuses and an excellent benefit package too! You'll have comprehensive insurance plans, HSA option, continuing education fund, malpractice insurance, paid-time-off, paid holidays and 401(k).

LPN Clinical Research Coordinator

• Works under the direction of the study manager
• Schedules subject’s appointments
• Conducts and assists with the informed consent for clinical trials
• Reviews and develops a familiarity with the protocols and, e.g. clinical trial proceedings and timeline, inclusion and exclusion criteria, schedule of events, confidentiality and privacy protections.
• Creates and maintains source documents
• Reviews and edits data to ensure completeness and accuracy of information; follow up with subjects to resolve problems or clarify data collected. Assure timely completion of case report forms.
• Tracks log such as temperature logs, screening/enrollment logs, and drug/device logs/accountability. Maintains adequate inventory of study supplies, responsible for timely shipment of all lab supplies.
• Responsible for handling investigational drugs/devices, follows the sponsor protocol and investigational drug/device accountability.
• Performs miscellaneous (administrative) job-related duties as necessary
• Prepares for monitoring visits
• Maintains study timelines
• Attends investigator meetings as needed
• Screens patients and phone calls for emergent/urgent situations. Obtains pertinent information and tests for physicians. Triages patient complaints.
• Adapts to situations as needed.
• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, document each potential participant’s eligibility or exclusion.
• Documents per protocol and follows any AE/SAE’s collected during the study.
• Responsible for ensuring study is compliance with local and federal laws and regulations.
• Creates and maintains all documents and records related to the study.
• Able to effectively communicate and discuss clinical trial enrollment with patients and