What are the responsibilities and job description for the Clinical Research Coordinator position at Eye Care Specialists?
Overview
At Vision Innovation Partners, we exist to protect and restore vision. Because Vision is our Mission, everyone at VIP focuses on providing great patient outcomes and experiences. A career at VIP provides opportunities for growth and development, and a culture centered on our Shared Values – PATIENTS.
(Clinical Research Coordinator), You'll join a team of innovative and accomplished providers, surgeons, and clinical care staff.
Responsibilities
What You Will Do:
- 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.
Qualifications
What we offer:
- Competitive compensation package
- Excellent comprehensive benefits
- 401(K)
- Significant eye care discounts
- Continuing education allowances
- Career growth and development
- PTO and holidays off
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.