- Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
- Prepare visit-specific documentation and charts for Clinical Research Coordinator
- Observe Coordinator in patient care and management
- Assist Coordinator in monitoring subject flow and assist in subject care and management
- Observe, assist, collect and record all necessary data for follow up (e.g. adverse events, concomitant medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy)
- Transcribe subject study information from source documents to the Electronic Case Report Forms
- Administer all mandatory questionnaires to study subjects
- Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol
- Promptly request all necessary medical records for Serious Adverse Event Reporting
- Process and ship laboratory biological samples for analysis
- Perform intraocular pressure checks after injections
- Perform trial frame refraction and ETDRS visual acuity testing (For ISTs only, at selected sites)
- Inform subjects and obtain written re-consents in regard to ICF's
- Applicants MUST be personally motivated to provide excellent patient care
- 1+ years of clinical trials research assistant experience in a retina or general ophthalmology environment preferred
- Knowledge of medical terminology
- Be an excellent team player who works cooperatively and respectfully with all doctors, supervisors and co-workers
- Displays a desire to perpetually "Learn and Grow"
- Efficient and highly accurate user of applicable information technology and health care management systems
- High School Degree or GED
- Paid Holidays - 7 days per year
- Personal Time Off (PTO) - 16 days per year
- Health Insurance
- Health Reimbursement Account
- Health Savings Account
- Dental Insurance (free single coverage)
- Flexible Spending Accounts
- Basic and Supplemental Term Life Insurance (free single coverage)
- Long Term Disability (free single coverage)
- Long Term Care (free single coverage)
- Short-Term Disability
- Vision
- Annual $250 uniform (scrubs and shoes) reimbursement
- We exist to serve our patients. We will provide the best available medical skills, technology, and service. We will be their advocates. We will care for our patients as if they were members of our family. We will treat our patients with respect, dignity, and kindness.
- We are proud of our dedicated staff. We will strive to provide a rewarding career with opportunity for personal and professional growth. We will promote teamwork. We will provide a respectful and safe working environment.
- We are humbled that other doctors entrust their patients to our care. We will be available when we are needed. We will promptly communicate the results of patient evaluation and treatment. We will respect the referring doctors' relationships with their patients.
- We recognize that we have a responsibility to our community. We will strive to be desire to perpetually "Learn and Grow"
- Efficient and highly accurate user of applicable information technology and health care management systems
- A good corporate citizen. We will function ethically. We will be prudent in our stewardship of healthcare resources.
- Medical advances are critical to our patients. We will remain at the forefront in the search for new knowledge and treatments of retinal disease. We will participate in clinical research. We will share our knowledge with our patients and referring doctors, and with our retinal colleagues around the world.
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Clinical Trials Research Assistant - Minneapolis, United States - Vitreoretinal Surgery PLLC
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Job DescriptionApply Here:
We are seeking multiple outgoing, patient focused individuals to work as Clinical Trials Research Assistant at our Retina Consultants of Minnesota Edina, MN clinic.Responsibilities for an Clinical Trials Research Assistant include: