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

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

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

Practices in accordance with all federal and state regulations, DFCI policies and Joint Commission standards. Responsible for designated daily operations and/or clinical activities of assigned area. Appropriately dispenses pharmaceuticals, including sterile products, chemotherapy, biologics, controlled substances, and investigational medications. Evaluates all providers'

Oversight of research study 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 data q

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 Responsible for day to day oversight and management of assigned projects. Responsible for development and maintenance of Trial Master File (

With direct oversight, the Clinical Authorization Specialist Manages approval process for clinically complex cases Discusses complex medical necessity cases in all aspects of the prior authorization work (on label drug, off label drug, laboratory testing, and others as assigned) with attending physicians. Understands clinically complex medical situations and communicates

Provide exceptional customer support to DF/HCC stakeholders, including study teams, clinicians, Office of Data Quality, Office for Human Research Studies, Grants & Contracts, Mass General Brigham eCare and others by either resolving issues or facilitating connection with appropriate resources. Build protocol treatment arms and calendars in the clinical trial management sy

Conduct standardized biological or biochemical assays and laboratory analyses, eg. TR FRET, FP, western blot, cell based assays Maintains cell culture and optimizes protein purifications using various expression systems such as coli , insect and mammalian systems Compiles and analyzes experimental data and interprets results to write summaries of findings for presentation

Design, conduct, troubleshoot, and validate hypothesis driven and hypothesis generating experiments using in vitro and in vivo approaches. Maintain detailed and understandable lab notebooks and records. Mentoring of research technicians and undergraduate students. Interpret, discuss, and present research findings with lab members and principal investigator. Perform and su

Quality Assurance Duties (~4 days/week) Conducts observations of technicians for quality and accuracy of aseptic technique and practice for compliance with applicable policies. Administers required validations of employees such as media fill tests and fingertip testing at all pharmacy locations as required. Performs other testing in accordance with USP, Board of Pharmacy,

Ensures proper patient identification and maintains patient safety, privacy, confidentiality and follows guidelines under HIPAA. Obtains and records vital signs, pain screens, weights and heights accurately into Electronic Medical Records (EMR). Reports changes and/or abnormalities in vital signs; findings that are outside of defined parameters; and changes in patient's c