Prepare or assist in preparing consent forms, continuation review reports, protocol modifications, serious adverse event reports, and other study reports.
February 28, 2020
ACTIVELY ENGAGES IN PRACTICE AND ORGANIZATIONAL INITIATIVES THAT CREATE AND MAINTAIN AN INTERNAL ENVIRONMENT THAT IS SAFE, HAZARD-FREE, ERGONOMICALLY CORRECT, CONFIDENTIAL, AND COMFORTABLE FOR PATIENTS, VISITORS, AND STAFF.
March 23, 2020
Provides regulatory affairs training and mentorship to IDCRP study teams and regulatory affairs support personnel throughout the network, this may include remote training or travel to meet with and train study teams located at the PCC and throughout the IDCRP clinical study site network as needed.
April 16, 2020
Participates in research related programs, such as the Clinical/translational Research Staff Council and its activities by submitting issues or suggesting solutions, and reviewing Council information, by attending meetings open to research staff and by sharing information with other research personnel.
May 01, 2020
Assists the physician in providing medical care to patients of various ages according to the policy of individual practice, in accordance with professional standards and hospital policies and procedures.
May 27, 2020
Maintains knowledge of patient eligibility requirements for additional services and assists patients in navigating their care with both in house and outside providers by facilitating scheduling of visits, identifying barriers to receiving care, and assisting with providing referrals to community and internal resources.
May 27, 2020
Develop interventional strategies to maximize appropriate antibiotic utilization and improvement in patient outcomes included but not limited to antibiotic guidelines, clinical pathways, restriction criteria, policy development, new laboratory methods and formulary management.
June 04, 2020