University of Maryland, Baltimore
Clinical Research Specialist
University of Maryland, Baltimore, Baltimore, Maryland, United States, 21276
University of Maryland, Baltimore Clinical Research Specialist Baltimore, Maryland Apply Now
The University of Maryland, Baltimore (UMB) Marlene & Stewart Greenebaum Comprehensive Cancer Center (UMGCCC) has an exciting opportunity for a full-time Clinical Research Specialist for the Solid Tumor research program. Following an extensive training program, the Clinical Research Specialist will be assigned a portfolio of cutting-edge novel therapeutic trials and will be the primary interface, along with the faculty member, for cancer patients enrolled in the studies. The Clinical Research Specialist 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 Research Specialist is also responsible for data collection, resolving standard of care issues and direct research support. This full-time position works Monday through Friday, and work scheduling flexibility that includes working outside of normal working hours is highly preferred. 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 that must be selected and is effective on your date of hire. Exempt regular staff receive a generous leave package that includes over 4 weeks of vacation accrued each year, paid holidays, 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). Essential Functions: Performs as a single Specialist in a clinical setting who is responsible for providing technical expertise to research programs and projects overseeing clinical research activities. Coordinates the preparation of Institutional Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPAA) protocol development and ensures compliance of research operations with protocols. Manages interaction with subject participants including eligibility screening, recruitment, enrollment, ensuring informed consent is properly secured and documented, counseling, and obtaining patient medical history. Establishes and maintains database files and reports using computer applications such as Microsoft Excel/Access. Performs data checks, audits, and data cleaning. Checks validity and accuracy of data ensuring compliance with quality control requirements and study relevance. Performs clinical research activities including advanced data analysis using statistical software such as SAS, SPSS, and R; data management (collection, entry, verification); data interpretation, and ensures compliance and clinical relevance of data. Maintains communication with participants and colleagues regarding protocol specific information and research orders. Serves as liaison to other departments such as IRB or CCT, outside organizations, government agencies, and product representatives to promote effective and efficient operation and use of resources. Oversees and coordinates the day-to-day clinical research operations, study initiation, execution, and completion. Performs day-to-day operational duties such as monitoring the budget; budget negotiation and review, ensuring quality control and safety compliance; serving as liaison with IRB, submitting invoicing, developing policies, procedures, and/or methods for laboratory experimentation; and ordering supplies. Searches relevant literature, develops conclusions on research findings, writes reports, prepares and delivers presentations of relevant findings and conclusions, and recommends appropriate actions. Provides training to less experienced researchers; assisting in developing and submitting grants, papers, abstracts, manuscripts and presenting studies; developing protocol manuals and data collection instruments; participating in field visits, responding to requests and questions from individuals, institutions, government agencies, and funding agencies; and participating in the design of research studies. Performs other duties as assigned. Education:
Bachelor's degree in a scientific field of study or related to the research of the clinical setting. Experience:
Three (3) years of clinical research including two (2) years in the relevant research specialization. Prior experience with patients and patient interaction preferred. Other:
May consider a combination of directly related experience and education. Some schedule flexibility is highly preferred. 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 HIPAA regulations. Hiring Range:
$62,000 - $73,000, commensurate with education and experience. UMB is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law or policy. For assistance related to employment, please contact the Talent Recruitment department at HRJobs@umaryland.edu. 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 a UMB Job Applicant Accommodation Request. 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 the UMB Notice of Non-Discrimination for more information. Job:
Reg or CII Exempt Staff
*Organization:
School of Medicine - Marlene and Stewart Greenebaum Comprehensive Cancer Center
*Title:
Clinical Research Specialist
Location:
null
*Requisition ID:
240001FU
#J-18808-Ljbffr
The University of Maryland, Baltimore (UMB) Marlene & Stewart Greenebaum Comprehensive Cancer Center (UMGCCC) has an exciting opportunity for a full-time Clinical Research Specialist for the Solid Tumor research program. Following an extensive training program, the Clinical Research Specialist will be assigned a portfolio of cutting-edge novel therapeutic trials and will be the primary interface, along with the faculty member, for cancer patients enrolled in the studies. The Clinical Research Specialist 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 Research Specialist is also responsible for data collection, resolving standard of care issues and direct research support. This full-time position works Monday through Friday, and work scheduling flexibility that includes working outside of normal working hours is highly preferred. 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 that must be selected and is effective on your date of hire. Exempt regular staff receive a generous leave package that includes over 4 weeks of vacation accrued each year, paid holidays, 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). Essential Functions: Performs as a single Specialist in a clinical setting who is responsible for providing technical expertise to research programs and projects overseeing clinical research activities. Coordinates the preparation of Institutional Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPAA) protocol development and ensures compliance of research operations with protocols. Manages interaction with subject participants including eligibility screening, recruitment, enrollment, ensuring informed consent is properly secured and documented, counseling, and obtaining patient medical history. Establishes and maintains database files and reports using computer applications such as Microsoft Excel/Access. Performs data checks, audits, and data cleaning. Checks validity and accuracy of data ensuring compliance with quality control requirements and study relevance. Performs clinical research activities including advanced data analysis using statistical software such as SAS, SPSS, and R; data management (collection, entry, verification); data interpretation, and ensures compliance and clinical relevance of data. Maintains communication with participants and colleagues regarding protocol specific information and research orders. Serves as liaison to other departments such as IRB or CCT, outside organizations, government agencies, and product representatives to promote effective and efficient operation and use of resources. Oversees and coordinates the day-to-day clinical research operations, study initiation, execution, and completion. Performs day-to-day operational duties such as monitoring the budget; budget negotiation and review, ensuring quality control and safety compliance; serving as liaison with IRB, submitting invoicing, developing policies, procedures, and/or methods for laboratory experimentation; and ordering supplies. Searches relevant literature, develops conclusions on research findings, writes reports, prepares and delivers presentations of relevant findings and conclusions, and recommends appropriate actions. Provides training to less experienced researchers; assisting in developing and submitting grants, papers, abstracts, manuscripts and presenting studies; developing protocol manuals and data collection instruments; participating in field visits, responding to requests and questions from individuals, institutions, government agencies, and funding agencies; and participating in the design of research studies. Performs other duties as assigned. Education:
Bachelor's degree in a scientific field of study or related to the research of the clinical setting. Experience:
Three (3) years of clinical research including two (2) years in the relevant research specialization. Prior experience with patients and patient interaction preferred. Other:
May consider a combination of directly related experience and education. Some schedule flexibility is highly preferred. 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 HIPAA regulations. Hiring Range:
$62,000 - $73,000, commensurate with education and experience. UMB is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law or policy. For assistance related to employment, please contact the Talent Recruitment department at HRJobs@umaryland.edu. 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 a UMB Job Applicant Accommodation Request. 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 the UMB Notice of Non-Discrimination for more information. Job:
Reg or CII Exempt Staff
*Organization:
School of Medicine - Marlene and Stewart Greenebaum Comprehensive Cancer Center
*Title:
Clinical Research Specialist
Location:
null
*Requisition ID:
240001FU
#J-18808-Ljbffr