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Research Technician No supervisory responsibilities. Normally receives detailed instructions on all work. Qualifications Bachelor's Degree with a major in chemistry required. Research experience (> 1 yr) in organic chemistry or medicinal chemistry strongly preferred. Experience with compound characterization with LC MS and NMR preferred. Experience with using chemistry la
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The laboratory investigates transcriptional and epigenetic control of cell fate, stem cell biology, and cancers in the mouse and human digestive tract. Our basic research in these areas generates large volumes of data from ChIP seq, ATAC seq, RNA seq, and related studies of primary stomach and intestinal cells. Computational analysis of these data is necessary at two leve
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A research assistant position is available to join the Hill Laboratory in the Department of Medical Oncology at Dana Farber Cancer Institute (https //hilllab.dana farber.org/). We are looking for an enthusiastic scientist to work on our existing and upcoming projects. Our group studies the way ovarian and endometrial cancers respond to therapy and how the entire tumor cha
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Management of Scientific Project Deliverables and Timelines Ensure success of project milestones associated with the various grants and research efforts. Lead the implementation of complex research projects, with focus on timelines and deliverables. Maintain expertise on advances in the field and provides scientific input on ideas and project direction. Integrate activiti
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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
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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
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We are seeking a highly motivated individual to coordinate our collaborative studies that are dependent on receiving, processing, and profiling patient samples collected from numerous multi institutional trials. These trials originate both from Dana Farber Cancer Institute as well as national clinical trial consortiums. We expect all the responsibilities associated with t
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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
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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
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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
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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
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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
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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
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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
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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
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