Develops and manages comprehensive budgets for clinical research studies at the NMRC CTC. Establishes and manages a variety of contracts/agreements for executing clinical research studies at the NMRC CTC. Forecasts personnel, supply, equipment, space, and service needs for executing clinical research studies at the NMRC CTC; drives and/or supports efficient, effective, an

Management and Oversight of Proposal Efforts Manage all aspects of the proposal response by identifying proposal support personnel, developing schedules and writing templates, planning/coordinating meetings, and preparing/collecting partner data calls. Guide proposal/technical writers in developing compliant sections that clearly articulate the win strategy. Review, edit,

Maintains compliance with established laboratory safety and other procedures. Ensures the proper disposal of infectious and hazardous materials. Applies quality control measures as outlined/required by the protocol. Provides basic data analysis. Performs laboratory research projects, including collection and organization of data, and maintaining databases. Makes detailed

Performance of serological screening assays for the detection of HIV in a high throughput laboratory, as well as performing specimen processing duties in accordance with laboratory SOPs, manufacturer guidelines and CAP/ FDA regulations . Ensures proper handling of samples, data entry, aliquoting of sampless for storage, retrieval of samples and themonitoring of laboratory

Interact directly with Principal Investigators, Investigators, Clinical Research Coordinators, and other protocol team members to develop and document DCAC requirements for support of data management as primary study clinical data manager. Design and maintain data entry screens and data management. Drafts and oversees execution of study validation. Develop, plan, and coor

Design experiments and performs laboratory procedures to achieve specific aims and complete project deliverables within scheduled time frame. Keeps good record of experimental data, and perform data analysis, interpretation in a timely manner. Regularly communicate with project leader to provide research progress and share results with other scientists in the laboratory o

Maintains supervisors' calendar and coordinates various staff meetings and events. Plans and coordinates large meetings. Ensures the presenter is provided with relevant information and all logistical and technical preparations have been made for the presentation. Drafts and proofreads letters and PowerPoint presentations on behalf of the VP, USU Portfolio. Provides excell

In assistance to the Principal Investigator and the Senior Staff Scientists of the Biological Defense Research Directorate, the incumbent is responsible for conducting molecular biological techniques necessary for the design, construction and production of PCR and biosensor based molecular assays for the rapid detection and diagnosis of various biological or infectious ag

Performs bioinformatics analysis of molecular profiling data such as DNA whole genome sequencing, spatial transcriptomics, gene panel sequencing. Assists in developing multi omics hypotheses for research questions, with statistical testing procedures and graphical displays. Analyzes data and results for presentations at scientific meetings and for publication in journals.

The incumbent works as a clinical pharmacist in an outpatient/inpatient setting in support of the Murtha Cancer Center Research Program & Hem/Onc clinics. As a clinical pharmacist, the incumbent supports a full scope of healthcare services for patients with both acute and chronic illnesses and conditions managing the entire spectrum of pharmacotherapy. The Clinical Pharma

Performs post award activities including award financial management, award restriction monitoring, compliance monitoring, and timely report submission. Responsible for award set up activities including negotiating agreement with sponsor, award set up, and providing award management procedures and requirements to Principal Investigator (PI) and Program Managers (PM). Respo

Provides substantive, structural, and copy edits of analytical manuscripts for organization, completeness, accuracy, and compliance with language, style, and formatting. Works closely with Agency historians, archaeologists, and analysis throughout the editing process. Develops style guides that adhere to Agency standards. Reviews the reports for compliance with the langua

Adhere to a policy of strict confidentiality concerning all documents, data, and information maintained within the department. Adhere to department Standard Operating Procedures for all data management / programming responsibilities. Provide programming for data extraction, edit logic checks, data listings, summary statistics, analyses, reports, tabulations, creation of a

Support genetic counselors' and clinical geneticists' clinical activities through the clinical cancer genetics program at MCC. Coordinate with genetic counselors and clinical geneticists the hereditary cancer genetic risk assessment process and daily clinical needs of the clinical cancer genetics program. Coordinate and assist with all aspects of genetic testing researchi

In assistance to the Principal Investigator and the Senior Staff Scientists of the Biological Defense Research Directorate, the incumbent is responsible for conducting molecular biological techniques necessary for the design, construction and production of PCR and biosensor based molecular assays for the rapid detection and diagnosis of various biological or infectious ag