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

Create an exceptional patient experience by delivering outstanding customer service throughout the check in and check out process. Manage complex scheduling to meet patient needs. Act as a liaison for patients, families and providers. Respond to emergent and compliance matters with creative problem solving and critical thinking. Qualifications Bachelor's degree preferred.

Provide administrative and calendar management support for Pathway's pre review, review, and post review meetings Maintain communication between Dana Farber Pathways Administration and external vendor(s) with Pathway's schedule related updates Provide administrative and calendar management support to Dana Farber Pathways and Symptom Management including; the Senior Direct

Creates coverage analysis grids based on clinical trial protocol documents Researches and applies policies, guidance and guidelines from various sources including federal and state regulations. Applies clinical guidelines, Medicare regulations, and study team guidance of conventional care to independently determine which services are considered routine care Disseminates t

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

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

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

Screen patients for protocol eligibility, obtain informed consent, and register study participants to cohort studies. Interact with study participants as directed/required by the protocol and/or study team. Review and abstract clinical information from medical records for patients into departmental databases upon study enrollment and follow up. Verify data for quality and

Facilitate human research studies through sample and data collection and coordination. Utilize REDCap, OncCore, Excel and other hospital information systems and statistical software analysis tools to perform clinical research and outcomes data analysis for research publications. Manage various databases from multiple labs generating clinical and biological data of tumor a

Design and implement studies to evaluate determinants of pancreatic cancer risk and outcomes Collaborate with other laboratory members with expertise in epidemiology, biostatistics, pathology, molecular biology, and functional genomics Conduct analyses using statistical software, such as SAS, R, and others Participate in group meetings and work collaboratively on larger p

Commonly performed tasks will include tissue culture, bacterial cultures, DNA cloning, DNA editing with CRISPR/Cas9, FACS analysis, RNA extraction, real time PCR, sequencing, and different forms of microscopy. Accordingly, prior experience in molecular biology, cell biology or mammalian cell culture is helpful but not required; computational expertise and experience in co

Responsible for cell culture and performing drug treatments Prepares lab reagents and media Conduct standardized biological or biochemical assays and laboratory analyses, eg. TR FRET, FP, pull downs, cell based assays, western blot, flow cytometry Analyzes experimental data and interpret results to write reports, presentations, grant and publication preparation Uses compu