Orients and assists in training new staff. Qualifications Bachelor's Degree and 1 3 years of equivalent experience required. Experience working in a medical or scientific research setting or comparable technology orientated business environment preferred. COMPETENCIES Demonstrates understanding of CRF completion, including timely and accurate transcription of study data S

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries. Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Provide administrative support to Research Nurses in clinic setting. Responsible for basic clinical trial document preparation (informed consents, study drug diaries, surveys (electronic/paper), research specimen kits, etc.) Administer clinical trial related surveys and use validated tools to assess a trial participant's functional and cognitive abilities as required by t

Facilitate human research studies through sample and data collection and coordination. Utilize REDCap, OncCore, Excel and other hospital information systems and statistical software analysis tools to perform clinical research and outcomes data analysis for research publications. Manage various databases from multiple labs generating clinical and biological data of tumor a

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Serve as a study contact for a few longitudinal clinical research studies Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis. Screen, recruit, and enroll eligible patients and track participation over time (including some travel to Dana Farber's Londonder

Primary responsibility will include management and maintenance of clinical and research databases and assistance with chart and database abstraction. Recruitment and consent of patients for enrollment on research studies Oversight of the research study start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activati

Oversight of research study start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data q