Job Listing
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| Job ID: 14039054 |
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| How to Apply: | To see employer contact information, log in or register. |
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| Job Title: | Research Ophthalmic Assistant |
| Work Type: | Work Days: Weekdays, Work Vary: No , Shift: First (Day), Hours Per Week: 40, Work Type: Regular |
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| Salary Offered: | Unspecified |
| Benefits: | 401(k) or other retirement, Clothing/uniform allowance, Dental Insurance, Health Insurance, Holidays, Sick Leave or PTO, Vacation or PTO, Vision Plan |
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| Physical Required: | Unspecified |
| Drug Testing Required: | Unspecified |
| Education Required: | |
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| Experience Required: | Unspecified |
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| Required Skills: | Education & Licensing
• Bachelor’s Degree in business or healthcare required
Experience
• Prior experience in academic, ophthalmology, pharmaceutical, or medical device clinical trials required. 1-2 years minimum
• Working knowledge of research methodology and federal regulations applicable to clinical trials required, one year preferred. |
| Preferred Skills: |
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| Job Description: |
Position Summary
The Research Ophthalmic Assistant will provide direct support to the research program at Associated Eye Care. This position works closely with the providers, technicians, and research groups to provide clinical trial organization and support.
Research Ophthalmic Assistant Essential Functions
• Assisting with study initiation activities, such as coordinating the delivery of study-related paperwork, equipment, demos, supplies, and participating in study-initiation meetings.
• Overseeing and participating in patient recruitment, screening, scheduling, and informed consent activities.
• Serving as the primary patient contact in areas such as counseling the patient on visit requirements, study purpose, and study costs, etc. and providing high quality patient care by promptly addressing patient information needs.
• Preparing patient charts for patient visits, ensuring complete data collection, and assisting clinical research technicians with case report form completion as requested.
• Assisting in monitoring visits with sponsor staff (e.g., queries, source document reconciliation, preparing regulatory documents, answering questions)
• Ensuring protocol and regulatory compliance to assigned clinical study protocols.
• Serving as the primary liaison between clinical study sponsors, patients, and AEC staff regarding study protocol requirements and communicates clinical study information with study participants, physicians, clinical study project team, and clinical research manager in an appropriate format (e.g., meeting minutes, status reports, telephone calls, e-mails, memos, and letters).
• Maintaining study regulatory file and test article accountability per internal standards.
• Maintaining accurate clinical study electronic and hard copy documentation in accordance with clinical study protocols, applicable regulations, and departmental procedures.
• Assisting with report preparation and clinical study communications to external agencies (e.g., FDA, IRB) as requested.
• Participate in advanced training of new technology utilized for study purposes, willing to train clinic staff on this technology.
• Assisting with technician tasks based on study requirements.
• Representing clinical research department on internal project teams as requested.
• Ability to flex hours based on study volumes.
Other Essential Functions
• Must be willing and able to work a variety of hours and work in the various locations as needed. The locations include Hudson, Lino Lakes, New Richmond, Stillwater, Woodbury and any partner facility.
• Must be available to work outside of regular working hours on occasion and able to travel to other AEC offices as needed
• Must present self at the workstation, ready for work, at the scheduled time
• Participates in department and company meetings, as requested
• Provides quarterly updates on study
• Prepares a budget for the research department; set revenue and enrollment goals
• Other Duties as assigned
Refer to ID when applying |
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