OPEN RANK Clinical Research Assistant or Senior Clinical Research Assistant

University of Maryland, Baltimore-posted 6 days ago

$48,000 - $64,000/Yr

Full-time • Entry Level

Baltimore, MD

1,001-5,000 employees

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The Institute of Human Virology (IHV) is currently recruiting for a Senior Clinical Research Assistant or Clinical Research Assistant. This position will provide research assistant support for study(ies) implemented by the Research Initiative for Infectious Disease and Substance Use (RIIS). Benefits (Exempt Regular): 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, 15 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.

Responsible for facilitating and coordinating clinical research patient visits and data collection.
Assist 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.
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.
Coordinates paperwork for submission of IRB protocol, IRB amendments, and IRB continuing reviews.
Document 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.
Communicates directly with participants regarding the research study.
Perform data collection by conducting research interviews, reviewing medical charts, and accessing computerized medical information systems.
Independently establish and maintain database files and reports using computer applications such as Microsoft Excel/Access.
Perform data checks, audits, and data cleaning.
Check validity and accuracy of data ensuring compliance with quality control requirements and study relevance.
Assist the Principal Investigator and other research personnel in the development of research protocols and materials by providing study analysis and forming conclusions and recommendations.
Perform administrative duties such as: providing training and guidance to interviewers; 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.
Performs other related duties as assigned.

Bachelor's degree in a scientific field of study related to the research of clinical setting.
Knowledge of position requirements.
Knowledge of all applicable requirements, regulations, and laws.
Skill in effective use of applicable technology/systems.
Ability to effectively communicate both verbal and written thoughts, ideas, and facts.
Ability to work cooperatively with others and independently.
Ability to demonstrate, understand, apply, and adhere to the UMB Core Values of Respect and Integrity, Well-being and Sustainability, Equity and Justice, and Innovation and Discovery.
Two (2) years of experience in clinical research in research being performed in unit. (Senior Clinical Research Assistant)

Prior clinical research experience preferred. (Clinical Research Assistant)
May consider a combination of directly related experience and education.

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, 15 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
Flexible work schedules and teleworking options (if applicable per job).

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