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Senior Clinical Research Assistant
- University of Maryland, Baltimore (Baltimore, MD)
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*The Bone Marrow Transplant and Cellular Therapy (BMT-CT) research team within the Clinical Research Management Office of the University of Maryland, Baltimore School of Medicine, Marlene and Stewart Greenebaum Comprehensive Cancer Center (UMGCCC) is currently recruiting for a full-time Bone Marrow Senior Clinical Research Assistant.* ** Following an extensive training program, the Bone Marrow Senior Clinical Research Assistant will be assigned a portfolio of cutting-edge Chimeric Antigen Receptor T-Cell Therapy (CAR-T) and other novel therapeutic trials and will be the primary interface, along with the faculty member, for cancer patients enrolled in the studies. The Bone Marrow Senior Clinical Research Assistant will be responsible for screening, consenting, and enrolling patients as well as subsequently guiding them through procedures and visits required by the research protocol. The Bone Marrow Senior Clinical Research Assistant is also responsible for data collection, resolving standard of care issues and direct research support. The Bone Marrow Senior Clinical Research Assistant will interface directly with the Principal Investigators (PIs) on the protocols within their assigned portfolio as well as the medical care team, ancillary hospital staff, sponsor representatives, and data managers within UMGCCC. *Benefits Information* UMB offers a comprehensive benefits package that prioritizes wellness, work/life balance, and professional development, along with additional exciting perks that employees can take advantage of. This position participates in a retirement program (pension or optional retirement plan/ORP) that must be selected and is effective on your date of hire. Exempt regular staff receive a generous PAID leave package that includes over 4 weeks of vacation accrued each year, 16 paid holidays, 3 personal leave, unlimited accrual of sick time, and comprehensive health insurance; professional learning and development programs; tuition remission for employees and their dependents at any University System of Maryland school; and flexible work schedules and teleworking options (if applicable per job). *UMB is a public university and constituent institution of the University System of Maryland.**All employees are expected to work primarily physically within the State of Maryland.* ** *_Primary Duties:_* * Responsible for facilitating and coordinating clinical research patient visits and data collection. Supports the conduct of clinical trials, including the coordination of start-up activities, scheduling and preparing for patient visits, assisting with data collection and clarification, and general administrative duties. * Assists in the preparation of Institutional Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPPA) protocol development and ensure compliance of research operations with protocols. May assist in developing and recommending policies and procedures and/or design methods for clinical research activities. * Coordinates data collection of the research study including obtaining medical records, lab results, diagnostic results, visit notes, etc. Coordinates recruitment and screening subjects for research studies according to IRB approved protocols. May communicate directly with study participants. * Coordinates paperwork for submission of IRB protocol, IRB amendments, and IRB continuing reviews. Documents and report all adverse events as appropriate. * Participates in audits and monitor visits as needed according to policy. * Performs the coordination of data analysis and interpretation, and develops statistical reports of study data using descriptive statistics using SAS, STATA, and SPSSS software. Assists in developing, submitting, and providing content for grants, papers, abstracts, manuscripts, and presentations. Conducts and analyzes literature searches. Develops and establishes a database to track research data. * Coordinates development of research protocols and materials by providing study analysis and forming conclusions and recommendations. * Documents in accordance with state and federal standards pertaining to specific research participant enrolled in the study. Maintains communication with participants and colleagues regarding protocol specific information and research orders. Provides assessments and ensure protocol compliance while participants are in a study. * Performs other duties as assigned. *Education:*Bachelor's degree in a scientific field of study related to the research of the clinical setting. *Experience:*Two (2) years of experience in clinical research in research being performed in unit. Prior experience with patients and patient interaction preferred. *Other:*Except for qualifications established by law, additional related experience and formal education in which one has gained the knowledge, skills, and abilities required for full performance of the work of the job class may be substituted for the education or experience requirement on a year-for-year basis with 30 undergraduate college credits being equivalent to one year of related experience. In instances where specific education and/or experience is required only directly related education and/or experience may be substituted. *Knowledge, Skills, and Abilities* * Ability to understand and utilize scientific/medical terminology and research theory in both oral and written communications. * Ability to perform independent projects. * Ability to network with and provide information to key groups and individuals, and work as part of a team. * Knowledge of human subjects research, the regulations and policies surrounding it. * Ability to represent the Cancer Center and its faculty in a professional manner. * Ability to keep patient information confidential and possess knowledge of HIPPA regulations. ** *Hiring Range:*$55,500 - $59,000, commensurate with education and experience. UMB is committed to cultivating a diverse and inclusive workforce and is proud to be an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, ancestry or national origin, sex, pregnancy or related conditions, sexual orientation, gender identity or expression, genetic information, physical or mental disability, marital status, protected veteran's status, or any other legally protected classification. If you anticipate needing a reasonable accommodation for a disability under the Americans With Disabilities Act (ADA), during any part of the employment process, please submit aUMB Job Applicant Accommodation Request. You may also contact [email protected]. Please note that only inquiries concerning an ADA request for reasonable accommodation will be responded to from this email address. The University of Maryland, Baltimore prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to the Title IX Coordinator. Read theUMB Notice of Non-Discriminationfor more information. **Job:** **Reg or CII Exempt Staff* **Organization:** **School of Medicine - Marlene and Stewart Greenebaum Comprehensive Cancer Center* **Title:** *Senior Clinical Research Assistant* **Location:** *null* **Requisition ID:** *250000OG*
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Senior Clinical Research Assistant
- University of Maryland, Baltimore (Baltimore, MD)