No supervisory responsibilities. Normally receives general instructions on routine work, detailed instructions on new projects or assignments. Qualifications Bachelor's Degree required with a major in biology or chemistry preferred. Typically requires a minimum of 1 4 years related experience. Basic understanding of Mendelian inheritance concepts, mouse husbandry and need

The Senior Analyst, Client Services, Prospect Research provides prospect research, strategy and support for members of the Division of Philanthropy, a large fundraising office that raises over $300M annually in support of cancer research and patient care at Dana Farber Cancer Institute, the leading cancer hospital in New England. The Senior Analyst partners with Philanthr

Practices in accordance with all federal and state regulations, DFCI policies and Joint Commission standards. Responsible for designated daily operations and/or clinical activities of assigned area. Appropriately dispenses pharmaceuticals, including sterile products, chemotherapy, biologics, controlled substances, and investigational medications. Evaluates all providers'

Supports managers and employees, and acts as the direct day to day contact for employees in assigned client businesses Responds to a wide variety of questions and supports multiple service requests simultaneously. Has strong general knowledge of and effective working relationships with all HR functions, especially the Employee and Labor Relations Center of Expertise. Inte

Administrative Assists principal investigator with protocol development. Assists principal investigator as appropriate with the Institute's protocol review process. Assists the principal investigator in developing the protocol budget. Collaborates with the Dana Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific m

Create an exceptional patient experience by delivering outstanding customer service throughout the check in and check out process. Manage complex scheduling to meet patient needs. Act as a liaison for patients, families and providers. Respond to emergent and compliance matters with creative problem solving and critical thinking. Qualifications Bachelor's degree preferred.

Provide administrative and calendar management support for Pathway's pre review, review, and post review meetings Maintain communication between Dana Farber Pathways Administration and external vendor(s) with Pathway's schedule related updates Provide administrative and calendar management support to Dana Farber Pathways and Symptom Management including; the Senior Direct

Creates coverage analysis grids based on clinical trial protocol documents Researches and applies policies, guidance and guidelines from various sources including federal and state regulations. Applies clinical guidelines, Medicare regulations, and study team guidance of conventional care to independently determine which services are considered routine care Disseminates t

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

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

Screen patients for protocol eligibility, obtain informed consent, and register study participants to cohort studies. Interact with study participants as directed/required by the protocol and/or study team. Review and abstract clinical information from medical records for patients into departmental databases upon study enrollment and follow up. Verify data for quality and