Receiving general direction from the Security Supervisor, the Security Officer ensures a safe and secure environment, provides protective service and response for protection of the people and property of the Institute, and is responsible for assisting with the day to day operation of Department. Provides protection to people and property through patrol, investigation, mon

Provides a high level of customer service by interacting with patients, visitors and staff in a professional manner that is proactive, friendly and helpful Welcomes and acknowledges visitors, patients, and staff; provides information and directions to patients and visitors; anticipates the needs of others. Assists individuals with disabilities and/or mobility issues with

Plans sessions including selecting appropriate music and movements according to participants' capabilities. Monitors participants' progress and provides correction or adaptations as needed. Teaches proper breathing techniques used during physical exertion. Ensures a safe environment by maintaining equipment and supplies in a clean, operable and safe manner. Adheres to all

The HIM manager oversees day to day HIM operations, ensuring compliance with regulatory standards, providing leadership to a team of HIM professionals, and actively participating in the ongoing and annual evaluation of staff. Daily operations may include records processing, scanning and indexing, incomplete records and physician notification, deficiency analysis, transcri

Strategic Planning and Implementation Work with the Department Chair to implement goals for the Department. Coordinate faculty recruitment, including offer letters. Communicate with department faculty and staff regarding Institute wide strategic initiatives and policies. Serve as a liaison to other departments and centers. Leadership of Departmental Administrative Team Re

Ensure the Sponsor Investigator and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures, including DFCI CTO Monitoring standards and guidelines. Adhere to the protocols' Data Safety Monitoring Plans; e.g. monitoring visit type, frequency, and required critical monitoring activities by utilizing moni

Process samples as indicated in provided lab manuals. Maintain all record keeping and Quality Control requirements as needed. Work with study teams for all sample processing procedures and manuals Work with study teams for all kit related requirements Work with Clinical labs for sample tracking and shared patient samples Work with couriers to send samples to external labs

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

At Dana Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are equally committed to diversifying our faculty and staff. Cancer knows no boundaries and when it comes to hiring t

For this Animal Research Technician position, the Walensky laboratory is seeking a skilled, motivated, organized, and intellectually curious individual with technical prowess who can expertly handle mice and perform animal husbandry, breeding and colony management, disease model development, treatment studies, tissue harvest and analysis, and technical procedures (e.g., m

The Research Project Manager I will work independently under general supervision of a more senior manager within their disease group and or the Clinical Trials Office. This position may be responsible for some or all of the following 1. Responsible for day to day oversight and management of assigned projects. 2. Responsible for development and maintenance of Trial Master

Participates in day to day operations of the program including patient education and call triage Participates in program evaluation and development of strategic goals consistent with DFCI's mission and professional values. Participates in the QA/QI projects for the program. Supports the research activities of the program. Exhibits professional commitment through individua

Independently plan, manage, and perform biochemical experiments. Develop project proposals, timelines and resource needs, working closely with the Portfolio Manager and leadership. Monitor milestones and ensure deliverables are completed on time. Collect and analyze experimental data and identify next steps based on outcomes. Train research technicians and other scientifi

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