The OHS Admin Support Specialist provides superior customer service to all new and existing Dana Farber employees who visit the Human Resources and Occupational Health office. This role is the welcoming ambassador to the department and is responsible for providing administrative and onboarding support to HR, in addition to back …
The Cell Manufacturing Quality Specialist III is responsible for managing the activities of multiple quality improvement and change management initiatives to ensure that systems are safe, effective, appropriate, compliant, current and adhered to by CMCF staff. The Cell Manufacturing Quality Specialist III understands and applies principles of quality management practices …
The Cell Manufacturing Quality Specialist II independently monitors operations and quality improvement initiatives by gathering and reviewing quality data and preparing reports to assist in ensuring that systems are safe, effective, appropriate, compliant, current and adhered to by CMCF staff. The Cell Manufacturing Quality Specialist II builds understanding of quality …
Working in a fast-paced, high volume, dynamic environment, the Clinical Authorization Specialist will bring clinical expertise to the prior authorization and appeals processes and serve as a liaison and patient advocate between Dana Farber Cancer Institute and various health plans. Reporting to the Prior Authorization Supervisor , the Clinical Authorization …
The Patient Representative (PR) is the “first impression” a patient has of Dana-Farber Cancer Institute (DFCI). As the first point of contact, this role is critical to a patient’s experience and their entry into the DFCI system. PRs provide call center and administrative support for aspects of patient care within …
Under close supervision, provides emergency response to a variety of situations and incidents to support the department, patients, clinicians and/or faculty. Provides protection to people and property through patrol, investigation, monitoring alarms, and surveillance cameras. Provides a high level of customer service by interacting with patients, visitors, and staff in …
This position is fully onsite Monday through Friday from 3-11pm. Under close supervision, provides emergency response to a variety of situations and incidents to support the department, patients, clinicians and/or faculty. Provides protection to people and property through patrol, investigation, monitoring alarms, and surveillance cameras. Provides a high level of …
This is a Per Diem position is fully onsite and requires the ability to cover any shift. The primary post will be at our main campus (Longwood) but will need to have the flexibility to cover shifts at our regional campuses (South Shore Hospital, Merrimack Valley, and Londonderry, NH). It …
The Regulatory Coordinators (RC) works under the direction of the Breast Oncology Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory …
The Clinical and Translational Investigation Program (CTIP) was established in 2010 to centralize and standardize conduct of clinical research within the Dana-Farber/Boston Children’s Cancer and Blood Disorders Center. The mission of CTIP is to provide comprehensive infrastructure to collaborating investigators who conduct clinical and translational research relevant to children with …
This position's work location is remote, with occasional time onsite as needed. The selected candidate may only work remotely from a New England state (ME, VT, NH, MA, CT, RI). The Research Compliance Associate I, COI supports the Institute’s robust research conflicts of interest and industry interactions program. Contributes to …
Under the direction of the Vice President Quality and Patient Safety, the Director of Care Delivery Innovation is responsible for overseeing the resources and portfolio of the Care Delivery Innovation team. This role involves close collaboration with Institute and department leadership, as well as key stakeholders to prioritize, plan, implement, …
Read more about ""The Cell Manufacturing Quality Specialist II independently monitors operations and quality improvement initiatives by gathering and reviewing quality data and preparing reports to assist in ensuring that systems are safe, effective, appropriate, compliant, current and adhered to by CMCF staff. The Cell Manufacturing Quality Specialist II builds understanding of quality …
Read more about ""The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and …
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