Responsible for effective and efficient scheduling of clinical trial or protocol patients and/or transplant donors for clinical services and other resources, including but not limited to exam and infusion clinics, donor services, donor network centers, apheresis facilities, cellular product laboratory processing, financial counselor support, care coordination, social work

The postdoctoral fellow will work on HIV 1 env vaccine development and modulation of B cell affinity maturation.He or she will explore humoral and cell mediated autoimmune responses induced by vaccination and underlying mechanisms of breaking immune tolerance. Mouse model immunization studies, immune sera analyses, FACS for immune cells analyses, B cell repertoire analysi

Under moderate supervision, responsible for routine customer service and follow up activities Coordinate all account activity when balance becomes patient responsibility, including communication with the patient and, if applicable, guarantors and collection agencies through Emails, Phone calls/voice mails, MyChart messages (Epic in basket). Coordinate collections referral

Provides direct oversight of front line staff within their respective modality (e.g., Imaging Supervisor of CT provides oversight of CT technologists). Front line staff members will report to the Imaging Manager of their respective modality (e.g., CT technologists report to the Imaging Manager). PATIENT CONTACT Direct patient contact. The Imaging Supervisor is expected to

Responsible for light typing, basic document preparation, data entry, and may handle mass mailing projects. Responsible for scheduling meetings for individuals supported, including conference room scheduling. Coordinates travel arrangements for individuals supported, as well as laboratory personnel, postdoctoral candidates and visiting speakers. Responsible for the planni

Clinical Trials Operations Assistant Clinical Research Managers (ACRM) will be responsible for assisting the Clinical Research Manager with the oversight of their disease group's clinical trial portfolio and all related regulatory and compliance requirements. The ACRM will assist the CRM will all aspects of study start up, active and close out activities for the group's p

Responsible for immediately and effectively answering requests for interpretation throughout the Institute, with a priority for emergency and more urgent requests. Responsible for arriving on time to the appointments and to provide services from the point of entry throughout discharge. Interprets and transmits accurately and in understandable terms, complex medical inform

Assist team in the coordination of project related activities (ie. surveys/interviews) at internal or external (on site & off site) study sites. Contact, recruit and enroll research participants, as needed. Maintain databases (including data entry) and project documentation with accuracy, as needed. Maintain the security and confidentiality of all study materials and data

Conduct standardized biological, microbiological or biochemical tests and laboratory analyses, including the collection of information and samples from organic substances, such as blood, drugs, and animals. Isolate, identify and prepare specimens for examination. Analyze experimental data and interpret results to write reports and summaries of findings, including grant pr

None Qualifications Minimum Education High School diploma required. Physical Demands Ability to use computers, faxes, copiers and scanners. Able to lift 50 lbs. without restriction, ability to move wheeled equipment up to 250 pounds, climb step stool and carry boxes. This position requires a considerable amount of lifting and stocking of storage shelves to include, but no

Provides knowledgeable and skilled general administrative support to senior executives with Institute wide responsibilities. Duties may include Preparation of reports and other documents in accordance with specific timelines. Management of the executive's calendar. Representation of executive in specified areas as directed using a high level of discretion. Possession of 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

Evaluating and tracking the eligibility of all patients seen in the clinic for inclusion in various studies Responsible for consenting eligible patients in clinic. Administration of patient questionnaires in clinic and electronically. Reviewing and abstracting the medical records for patients. Entering the clinical data into the Clinical Research Information Systems (CRIS

Serves as the first point of contact and liaison for patients or referring providers by triaging calls and resolving questions directly whenever possible. Possesses a level of independence requiring knowledge of multiple disease specific programs. Provides administrative support and coordination for all aspects of patient care for patients, primarily focused on supporting

The Sustainability and Energy Engineer reports directly to the Senior Engineering Manager, within the Division of Facilities Management and Real Estate (FMRE). The position has overall responsibility for the implementation and engineering of the DFCI energy and sustainability programs in support of the Dana Farber Cancer Institute's Mission, core values, and strategic pla