DESCRIPTION

The Clinical Registry and Data Analyst II applies knowledge of clinical registry to collect, store, and report clinical data accurately and in accordance with regulatory agency requirements. Involves data collection, inputting and reporting to patient care data registries, often national. Implements methods for collecting, analyzing, storing, retrieving, reconciling, tracking, and reporting patient medical information and data.

Data reported in accordance with the requirements of federal, state and local laws, the standards of accrediting and regulatory agencies, and the requirements of study protocols. Assists in preparation for clinical trial subject visits, as well as possible clinical trial data entry. Participates in the collection, processing and shipment of biological samples, and maintenance of biobank, as needed. Assures maintenance of refrigerators/freezers where biobank samples are stored, and potentially other equipment. Other duties as assigned.

Professional who applies acquired job skills, policies, and procedures to complete substantive assignments/projects/tasks of moderate scope and complexity; exercises judgment within defined guidelines and practices to determine appropriate action.

MINIMUM QUALIFICATIONS

• Bachelor's Degree in business, healthcare administration or related area; and/or equivalent combination of experience/training.

• A minimum of two (2) years of related experience.

• Knowledge of and familiarity with the clinical and operational aspects of the clinical registry, including data collection, medical center policies, and regulatory requirements.

PREFERRED QUALIFICATIONS

• Hemophilia experience.

• ICD-10 coding experience.

• Basic knowledge of Excel.

• Experience with data collection, entry and reporting.

SPECIAL CONDITIONS

• Employment is subject to a criminal background check and pre-employment physical.