Responsibilities Facilitate human research studies through sample and data collection and coordination Utilize REDCap, OncCore, Excel and other hospital information systems and…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Primary responsibility will include management and maintenance of clinical and research databases and assistance with chart and database abstraction. Recruitmen…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Primary contact for the non-interventional study team which includes patient communication, referrals, management of cohort sample acquisition and collection, a…
Responsibilities Coordinate data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archivi…
Responsibilities Oversight of research study start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activiti…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and ar…
Responsibilities Screen patients for protocol eligibility, obtain informed consent, and register study participants to cohort studies. Interact with study participants as direc…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…