Research Assistant 2, HSS

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Overview

The Department of Emergency Medicine is looking to bring on a Research Assistant 2 to support recruitment and implementation of an NIH-funded clinical research study conducted in the Emergency Department. The Research Assistant 2 will participate in designated recruitment periods, including weekend coverage, until the study enrollment goal is reached.

Responsibilities include notifying Emergency Department clinicians of study activities; identifying potentially eligible participants through the electronic tracking board and collaboration with ED clinicians; approaching patients and introducing the study; assessing current alcohol and cannabis use; screening participants for eligibility using standardized instruments (AUDIT-C and CUDIT-R); obtaining informed consent; administering baseline and post-intervention research assessments; delivering the study Brief Negotiated Intervention (BNI); conducting 30-day follow-up assessments; entering and maintaining study data in REDCap; maintaining accurate research documentation; coordinating participant follow-up and electronic incentive distribution; and participating in weekly research meetings.

The Research Assistant 2 will work under the supervision of the Lead Research Associate and Principal Investigator and will be responsible for conducting study activities in accordance with study protocols, Good Clinical Practice, and applicable human subjects research regulations.

Job Duties

Recruit, screen, and enroll eligible Emergency Department (ED) participants according to study protocol.

Obtain informed consent and administer standardized research questionnaire and study assessments.

Deliver the study Brief Negotiated Intervention (BNI) following the approved intervention protocol.

Assist with data organization, coding, and quality review as directed. 

Conduct 30-day follow-up assessments and maintain participant retention (clinical research data collection and follow-up procedures).

Coordinate participant follow-up and distribute electronic participant incentives.

Participate in weekly research meetings and collaborate with the Lead Research Associate and Principal Investigator.

Work under the Lead RA for coordination and execution (team-based research coordination and support within structured protocols).

This position REQUIRES: occasional afterhours work as late as 12am midnight.

Required Skills and Abilities

1. Demonstrated experience obtaining informed consent. Demonstrated experience with participant recruitment. Proven ability to work with research protocols and clinical trials; adept at collecting and managing data.
2. Strong interpersonal skills, excellent written and verbal communication abilities, and experience working with diverse groups or patient populations.
3. Intermediate to advanced proficiency with Microsoft Office Suite (Excel, Word), electronic medical databases, and other relevant software.
4. Excellent organizational skills, attention to detail, and the ability to manage multiple tasks and priorities efficiently in a fast-paced environment.
5. Strong customer service orientation, with the ability to handle sensitive information confidentially and professionally.

Preferred Skills and Abilities

1. Bachelor's degree in a related field such as psychology, neuroscience, or public health; experience administering structured clinical interviews or managing research studies.
2. Familiarity with research regulations, ethical guidelines, and Institutional Review Board (IRB) procedures.
3. Proven experience with data management software, such as REDCap, OnCore, and clinical trial management systems (CTMS).
4. Prior experience in a clinical setting, working with subjects with psychiatric or cognitive disorders.
5. Completion of Good Clinical Practice (GCP) training, with certification as a Clinical Research Associate (CRA) or Clinical Research Professional (CRP) preferred.

PLEASE DISREGARD THE PRINICIPAL RESPOSIBILITES LISTED BELOW!!!

Principal Responsibilities

1. Researches and collects data through site or home visit intakes; library research; structured interviews; or through other means for research projects. 2. Interprets, synthesizes, and analyzes data using scientific or statistical techniques. Modifies and plans research experiments, procedures, tests, or survey instruments. Assists in research design. 3. Writes and edits material for publication and presentation. Reports on status of research activities. Oversees and instructs research and support staff on technical procedures, equipment operation, and laboratory maintenance. 4. Schedules and coordinates research activities. Identifies and recruits study participants. Orders and maintains inventory of supplies. 5. May assist in preparing financial information and monitoring budgets. 6. Performs additional functions incidental to research activities. Required Education and Experience Two years of related work experience in the same job family and a Bachelor's degree in a related field; or an equivalent combination of experience and education.

Job Posting Date

09/18/2026

Job Category

Technician

Bargaining Unit

L34

Compensation Grade

Labor Grade D

Compensation Grade Profile

Hourly Range

$31.83

Time Type

Full time

Duration Type

Staff Fixed Duration (Fixed Term)

Work Model

Hybrid

Background Check Requirements

All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.

Health Requirements

This role is a healthcare worker position. Healthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air.  HCW have specific health requirements that must be met prior to starting work, including MMR vaccine or immunity, varicella (chickenpox) vaccine or immunity, TB screening, COVID vaccine according to University policy, hepatitis B vaccine or immunity, and annual flu vaccination.

Posting Disclaimer

The hiring rate of a role is determined in accordance with the provisions outlined in the respective collective bargaining agreement.

The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-related duties through  their hiring department.

The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its faculty, staff, and student body qualified persons from a broad range of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual’s sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.

Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).

Note

Yale University is a tobacco-free campus.