Research Assistant, Clinical - SOM STAR Trauma Core

University of Maryland, Baltimore; Baltimore (MD); On-site; USD 42,000 - 64,000; Full time

Job summary

University of Maryland, Baltimore is seeking a Contractual Research Assistant, Clinical to support research projects in a clinical setting. You will recruit subjects, collect and organize data, and assist with analyses and manuscript preparation.

The role emphasizes data quality, adherence to IRB protocols, and collaboration with the PI and study team on multiple federally funded and industry-sponsored trials.

Qualifications

• Bachelor’s degree in epidemiology, sociology, psychology, biology, emergency health services, nursing or related field.
• Prior clinical research experience preferred.
• Knowledge of IRB processes and study recruitment.

Responsibilities

• Recruit and screen study subjects per IRB-approved protocols.
• Collect, verify, and manage data in study databases.
• Perform data analysis and produce descriptive statistics.
• Assist in developing grants, papers and presentations.
• Coordinate with PI and study personnel on protocol adherence.

Skills

Data collection

IRB compliance

Statistical interpretation

Communication

Teamwork

Education

Bachelor’s degree (epidemiology/related field)

Tools

SAS

STATA

SPSS

Excel/Access

Job description

Job Description

The Center for Shock Trauma and Anesthesiology Research/TraumaResearch in the School of Medicine is recruiting for a C1(contractual) Research Assistant, Clinical position. The position is responsible for assisting with the performance of research projects in a clinical setting, including recruitment of potential study subjects and collection and organization of data. The Research Assistant, Clinical is expected to work independently and knows and applies the fundamental concepts, practices and procedures of particular field of specialization. The position provides an exciting opportunity to work in a fast past environment on projects including federally funded studies and industry sponsored drug and device trials.

The position provides an exciting opportunity to work in a fastpast environment on multiple projects including federally fundedstudies and industry sponsored drug and device trials. The research may focus on any of the primary areas of research to include trauma resuscitation, traumatic brain injury, post traumatic complications, neuro-intensive care, clinical outcomes, critical care, sepsis, or acute lung injury.

This position is temporary full-time /non-benefitted. The selected candidate must be able to work rotating shifts which include nights, weekends and holidays. Only serious inquiries please.

Essential Functions

• Communicates directly with participants regarding the research study. Perform data collection by conducting research interviews,reviewing medical charts, and accessing computerized medicalinformation systems. Recruits and screens subjects for research studies according to IRB approved protocols. Verifies participant eligibility; obtains consent and enrollment; and assures accurate demographic information for follow-up.
• Independently establish and maintain database files and reportsusing computer applications such as Microsoft Excel/Access. Performdata checks, audits, and data cleaning. Check validity and accuracyof data ensuring compliance with quality control requirements andstudy relevance. Develops data collection instruments such assurvey questionnaires.
• Perform data analysis and interpretation and develops statisticalreports of study data using descriptive statistics using SAS,STATA, and SPSSS software. Assists in developing, submitting, andproviding content for grants, papers, abstracts, manuscripts, andpresentations. Conducts and analyzes literature searches.
• Assist the PI and other research personnel in the development ofresearch protocols and materials by providing study analysis and forming conclusions and recommendations. Assist in developing andrecommending policies and procedures and/or design methods forclinical research activities.
• Perform administrative duties such as: providing training andguidance to interviewers; participating in field visits, respondingto requests and questions from individuals, institutions,government agencies, and funding agencies; and participating in thedesign of research studies.
• Performs other related duties as assigned, such as maintaininginventory of bio specimens, and specimen collections andprocessing.

Qualifications - External

Minimum Qualifications

• Education: Bachelor’s degree in epidemiology, sociology, psychology, biology, emergency health services, nursing or field of study or science related to the research of the clinic.
• Experience: Prior experience in clinical research preferred.
• OR Consideration may be given for a unique combination of education and experience.*
• *Bachelor’s degree in an unrelated field with at least 18 credits in a field related to the research of the clinic or laboratory, as appropriate, or Bachelor’s degree in unrelated field with at least one year of experience in a field directly related to the research of the clinic or laboratory, as appropriate. 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 college credits being equivalent to one year of experience.
• Other: May require training related to occupational safety and health, environmental compliance, shipping of hazardous materials and/or ionizing radiation.

Knowledge, Skills, and Abilities

• Ability to understand and utilize scientific/medical terminologyand research theory in both oral and written communications.
• Ability to understand and apply approved guidelines of varyingresearch protocols.
• Knowledge of best practice in research protocols and procedures.
• Ability to gain knowledge and meet thereporting needs of UMB policies and practices for Institutional Review, Human Protections, Animal Protections and other the like.
• Ability to maintain high standards with the work being performed and maintain awareness with trends and influences.
• Assumes personalresponsibility for all outcomes; makes effective and timelydecisions; and learns how to effectively use technology.
• Skill in various interviewing techniques.
• Skill in data abstractionand entry into study specific database software applications.
• Skill in statistical interpretation and data analysis using statisticalsoftware as well as spreadsheet and database softwareapplications.
• Ability to effectively communicate both verbal and writtenthoughts, ideas, and facts.
• Writes and presents information in a clear and concise way.
• Interprets and understands writteninformation and is able to listen attentively to verbal andnon-verbal cues that lead to a deeper understanding.
• Ability to maintain confidentiality of subjects and information obtained.
• Ability to network with, and provide information to key groups and individuals.
• Ability to work as part of a team.
• Ability to work cooperatively with others and demonstrates professional, ethical, respectful, and courteous behavior when interacting with others.
• Capable of interacting pleasantly and positively with other to meet customer expectations, and provide follow up with customers.
• Ability to use measurable and verifiable information for making decisions or judgements.
• Excellent organizational and projectmanagement skills.
• Ability to use a consultative approach to resolve issues in area of responsibility.

Equal Opportunity Statement

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.

Reasonable Accommodation

If you need a reasonable accommodation for a disability, for any part of the recruitment process, please contact us at [e-mail] and let us know the nature of your request and your contact information. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

Responsibilities

• Responsible for assisting with the performance of research projects in a clinical setting, including recruitment of potential study subjects and collection and organization of data.
• ' Assist with performing data collection by conducting research interviews, reviewing medical charts, and accessing computerized medical information systems.
• Assists with recruiting and screening subjects for research studies according to IRB approved protocols.
• ' Assist in verifying participant eligibility; obtains consent and enrollment; and assures accurate demographic information for follow-up.
• ' Assist with data analysis and interpretation, and the development of statistical reports of study data using descriptive statistics using SAS, STATA, and SPSS statistical software.
• Assists in developing, submitting, and providing content for grants, papers, abstracts, manuscripts, and presentations.
• Conducts and analyzes literature searches.
• ' Assist the Principle Investigator and other research personnel in the development of research protocols and materials by providing study analysis and forming conclusions and recommendations.
• ' Assist in performing administrative duties.
• Maintains communication with participants and colleagues regarding protocol specific information and research orders.
• May also assist with providing assessments and ensuring protocol compliance while participants are in a study.
• ' Performs other duties as assigned.

Qualifications

Minimum Qualifications: Bachelor's degree in a scientific field of study related to the research of the clinical setting. Prior clinical research experience preferred. 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 may be substituted for the education or experience requirement. Knowledge, Skills, Abilities: Accomplishes responsibilities by applying specialized and theoretical knowledge, principles, and concepts of a professional discipline normally acquired through advanced education or specialized training. Resolves issues and significant matters on behalf of management by utilizing independent judgment, discretion, creativity, and analytical thinking. Contributes to development and evaluation of goals and objectives. Creates solutions to ensure legal and policy compliance. May supervise, mentor, or coordinate work of others (positions that supervise are responsible for service delivery, quality assurance, and employee performance). May independently manage or administer programs, processes, projects, or resources. Applies entry level knowledge, concepts, principles, and skills. Decision making occurs within defined parameters. Supervisor defines assignments, expectations, and deadlines. Supervisor may review work for quality. Demonstrates initiative and discretion to resolve routine and non-routine matters. 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.