Responsible for day to day oversight and management of assigned projects. Responsible for development and maintenance of Trial Master File (TMF), Assists PI with protocol and consent form development for initial application and with subsequent amendment changes. Initiates, plans, facilitates and oversees the research project start up, active and close out phases; for PI I

Responsible for day to day oversight and management of assigned projects. Responsible for development and maintenance of Trial Master File (TMF), Assists PI with protocol and consent form development for initial application and with subsequent amendment changes. Initiates, plans, facilitates and oversees the research project start up, active and close out phases; for PI I

Facilitate research operations by coordinating or carrying out tasks related to equipment, materials stocks, facilities, and shipping and receiving. Supports shipping and receiving for group or department. Assists with the maintenance of laboratory stocks, such as plastic and glassware. May carry out special research operations support such as preparing media. May assist

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

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

No direct supervision of others but does supervise assistive personnel as appropriate in the provision of patient care. Qualifications Licensed as a registered Nurse in the Commonwealth of Massachusetts, or New Hampshire as appropriate Baccalaureate degree in nursing strongly preferred. If associate degree in nursing, must complete BSN degree within 4 years Minimum of 1 y

Reviews and abstracts the medical records for patients. Entering the clinical data into the databases supporting the cohort studies within Breast Oncology. Ensures the proper entry of biospecimens into tracking systems across cohort studies. Retrieves archival tissue samples at outside institutions when relevant for translational studies. Coordinates the collection, proce

Disease Based RDS positions Responsible for reviewing and abstracting the medical records for research patients on trials they are assigned. Entering identified clinical data points in the corresponding database. Ensuring that data is entered within the outlined timelines for each trial. Assisting research teams with the development, testing and implementation of Case Rep

Agreements/Transactions Uses institutional templates to guide negotiations. In partnership with manager/senior staff, negotiates confidentiality agreements, material transfer agreements, data use agreements, multi site and academic collaboration agreements and amendments to the foregoing. May negotiate sponsored research agreements and non exclusive research reagent licen

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. Assist with logistical needs for intervention and/or evaluation activities, such as equipment set up, arranging food service and conference room scheduling. Assist with coordinat

Under general supervision, the Research Assistant I may be responsible for some or all the following Assist team in the coordination of project related activities (i.e., reports, creating presentations, leading multi site calls, etc.) Assist investigators in determining patient eligibility for studies; ensure eligibility criteria are documented on all patients and only el

Under general supervision, the Research Assistant II may be responsible for some or all of the following Contact, recruit, and enroll research participants. Collect and enter research data. Administer surveys/interview with research participants. Maintain databases (with emphasis on data entry) and project documentation with accuracy. Assist with documentation for and com

Under general supervision, the Research Assistant I may be responsible for some or all of the following Contact, recruit and enroll research participants. Collect and enter research data. Administer surveys/interview with research participants. Maintain databases (with emphasis on data entry) and project documentation with accuracy. Assist with documentation for and commu

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

Manage supportive care studies and maintain a comprehensive knowledge of study procedures. Use the electronic medical record to identify and screen patients for eligibility. Coordinating study visits with study patients and clinicians. Offer study participation to eligible patients, perform consent procedures, and collect baseline and follow up questionnaires. Maintain da