The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials.
KEY RESPONSIBILITIES:
- Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.
- Provides guidance to less experienced staff.
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JOB DESCRIPTION:
- With supervision, performs various laboratory procedures on patient specimens to assist in the diagnosis, study, treatment, or prevention of disease.
- Calculates and reports results.
- Performs preventive maintenance on laboratory equipment.
- Evaluates the validity of test results by comparing them to previous results and other laboratory data.
- Maintains complete and accurate documentation of patient information, test results, and equipment operation.
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The Workplace Accomodations Specialist serves as an interactive member of the Department of Accessibility Services to review supporting documentation and requests for accommodations from employees for quality, continuity, consistency and accuracy.
Orients, supports and provides guidance to employees and those in their support system(s) about the disability accommodations process, and appropriate use of accommodations.
KEY RESPONSIBILITIES:
- Reviews and determines eligibility for...
The Chief Counsel for Health Affairs (CCHA) will oversee all legal matters for Emory Healthcare. They also will serve as the primary legal advisor to the CEO, senior management team, Board of Directors, hospitals, and outpatient provider locations.
JOB DESCRIPTION:
- Under minimal supervision, performs a variety of specialized and complex research and laboratory tests and procedures.
- Uses independent judgment in applying or adapting scientific techniques.
- May assist in protocol design.
- Investigates and proposes alternative experimental procedures for consideration by a principal investigator.
- Assists in planning and scheduling research procedures.
- Analyzes and interprets results of studies....
JOB DESCRIPTION:
- Under the direct supervision of a registered radiopharmacist, assists in the production of radiopharmaceuticals for Positron Emission Tomography (PET) Human Research.
- Prepares human research radiopharmaceuticals in accordance with current Good Pharmacy Practice and USP<823> and USP<825> guidelines.
- Maintains proper operation of radiochemistry synthesis units to include post-production cleaning, preventative maintenance and repair....