Job Description

Job Description

Job Description

Ophthalmic Clinical Research Assistant

We are searching for a clinical research assistant to support our busy Ophthalmology research department. The Research Assistant provides administrative and clerical support to the Research Manager. The ideal candidate must be extremely organized with good critical thinking skills. They must be analytical and strong in communication skills to interact with trial participants, researchers, health care professionals and clinical trial sponsors. They must be competent with using computers and spreadsheets, with the ability to diligently follow protocol as required by the trial. Interested candidates should complete the Predictive Index at this link.
Education and Job Experience preferred:

• High school diploma or equivalent
• JCAHPO certification COA level or above or willingness to receive that certification with 6 months of employment
• BLS Certified
• GCP certification
• Infusion Therapy training preferred
• IATA training
• 2 years of ophthalmic experience
• Knowledge of procedures and diagnostics involved in an ophthalmic examination
• Willingness to participate in continuing education in the ophthalmic and clinical research fields

Required Skills/Traits:

• Follow written and verbal instructions
• Work independently; planning, organizing, scheduling and completing work within deadlines
• Multi-task, managing conflicting demands and priorities
• Strict adherence to HIPAA regulations
• Demonstrated attention to detail, accuracy and thoroughness
• Process and procedure oriented
• Highly organized and efficient
• Communicate clearly and professionally, both in oral and written correspondence
• Demonstrated consistency and dependability in attendance, quantity and quality of work
• Interacts professionally with managers, peers, patients and health-care providers
• Use of discretion regarding current, ongoing, or new projects in research and patient confidentiality and protection etc…

Specific responsibilities include:

• Assisting with routine data analysis and interpretation using data analysis programs
• Assisting in the setup, operation, and maintenance of research equipment/instruments
• Following established policies, procedures, and objectives, continuous quality improvement objectives, and safety, environmental, and/or infection control standards
• Recruiting subjects for trials and developing tools to improve clinical trial conduct
• Developing credible relationships with patients and providers
• Track documents and correspondence -- receive, print, scan and sort
• Ensure documents are complete and accurate, recognizing discrepancies and making corrections
• Compose and type routine correspondence and other documents
• Update/maintain database information
• Answer incoming phone calls to resolve patient inquiries, follow up as needed

PI08c0eb969f0d-25405-39341387

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