Laboratory Research Specialist or Lead Laboratory Research Specialist with (Sign on Bonus)
University of Maryland, Baltimore
- Baltimore, MD
- $56,000-67,000 per year
- Permanent
- Full-time
The Lead Laboratory Research Specialist position is eligible for a $4,000 sign-on bonus.
***Half will be paid following 30 days of satisfactory service at UMB, and half will be paid upon successful completion of probation. Current UMB employees are not eligible for the sign-on bonus.***Employees whose job duties require them to work in clinical settings or at clinical or field sites continue to be subject to the vaccine requirements of those sites. This position is required to be vaccinated against COVID−19. For additional information on protocols and exemptions, please visit the .Benefits: Exempt RegularUMB offers a that prioritizes wellness, work/life balance, and professional development. 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 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).Laboratory Research Specialist Primary Duties:
- Perform independent project(s) and participate in the design of research studies. Compile, analyze, and interpret research data using various relevant computer software applications including GraphPad Prism, SoftMax Pro, Microsoft Excel, etc.
- Independently perform ELISAs and multiplexed antibody assays with a high degree of precision to evaluate immune responses in samples collected from human volunteers enrolled in clinical trials. Independently perform other immunological assays (ELISpot), and measurement of antibody function.
- Assist with the development, optimization, and qualification of immunological assays for the testing of samples collected from human participants enrolled in clinical trials. Identify problems and collaborate on troubleshooting assay procedures.
- Analyze, organize, review, and interpret data collected from immunoassays. Critically evaluate research data and perform quality control.
- Communicate with study sponsors and both internal and external collaborators. Act as a liaison and point of contact for study sponsors and collaborators, responding to logistical and technical questions.
- Organize, manage, review, and ensure the highest quality of assay data. Prepare large data sets for submission. Upload assay data generated by the laboratory from clinical study specimens to the sponsor’s databases. Assure that all data is clean by following up on data discrepancies, missing information, and any required updates assigned by the sponsors.
- Promptly respond to any data queries.
- Conduct literature research and participate in editing and preparing manuscripts, reports, scientific illustrations, and computer graphics for publication. Contribute to the preparation of journal articles, grant proposals, and other research documents. Present research findings.
- Independently perform day-to-day laboratory research activities such as general housekeeping, maintaining inventory of supplies and reagents, processing biological samples, preparation of buffers and reagents, reconstituting and aliquoting of reagents, and thorough record keeping and documentation of activities.
- Assist with shipping biological specimens, generate study-related sample labels, and play a significant role in archiving specimens and maintaining inventories in the laboratory. This is a critical function for which organization, timeliness, and consistency are of utmost importance.
- Assist during the experimentation process.
- Administer day-to-day laboratory operations including monitoring the budget, ensuring quality control and safety compliance, developing policies and procedures, and ordering supplies. Actively participate in the establishment or revisions of standard operating procedures (SOPs) and multiple routine lab procedures.
- Maintain proper operation of research equipment, ensuring proper operation records, cleaning, ordering of required components, and explaining/resolving technical issues.
- Assist in the training of undergraduate and graduate students, post-doctoral, international fellows, and/or junior technical personnel in the performance of a variety of laboratory techniques.
- Perform other related duties as assigned.
- Independently develop, optimize, and qualify immunological assays for the testing of samples collected from human participants enrolled in clinical trials. Identify problems and lead the troubleshooting of assay procedures.
- Oversee and lead concurrent projects. Simultaneously track the progress of each study and ensure projects are on target to meet deadlines. Plan and schedule laboratory and administrative activities to meet study timelines. Generate careful and detailed budgets for projects and monitor funding and spending.
- Supervise, instruct, and guide up to four direct reports.
- Assemble and assist with literature research, editing and preparing manuscripts, scientific illustrations and computer graphics for publication. Conduct library research and prepares manuscripts, scientific illustrations and computer graphics for publication. Prepare material for journal articles and grant proposals.
- Knowledge of position requirements. Knowledge of all applicable requirements, regulations, and laws.
- Skill in effective use of applicable technology/systems. Proficiency in using Excel, GraphPad Prism, Word, PowerPoint, and Microsoft Teams and the ability to learn and adapt to new technologies, programs, and analysis software as needed.
- Knowledge of immunology is required. Some knowledge of immunoassays, assay development, and clinical trials is needed.
- Ability to effectively communicate both verbal and written thoughts, ideas, and facts. Ability to work cooperatively with others and independently.
- Ability to meticulously generate and maintain study-related spreadsheets. These include inventories associated with various types of clinical samples and study data generated by the laboratory. Ability to upload data generated by the laboratory and other information regarding specimens to the sponsor’s websites.
- Attention to detail, organizational skills, and critical thinking and troubleshooting skills are critical.
- Able to conduct bioanalytical method characterization. Excellent verbal and written communication skills are essential.