Research Associate

Salary Range $65,000.00 - $101,000.00 Job Requisition ID 133524WD Overview Carries out clinical research management and assignments for large‑scale human research studies and clinical trials. Responsible for recruiting, consenting and evaluating patients, conducting weekly clinical behavioral counseling sessions with participants, and enrolling participants into large‑scale research. Manages day‑to‑day operation of trials in alcohol and substance use disorder research, ensuring protocols are followed and updating and monitoring protocols at the Yale Stress Center. The Research Associate 2 serves as the primary interface between clinical, experimental, neuroimaging, and clinical trial studies. Required Skills and Abilities Excellent oral and written communication skills; ability to interact successfully with patients, staff, and faculty in a clinical research and academic environment. Strong clinical patient assessment skills, including conducting structured psychiatric diagnostic interviews. Ability to work independently as well as function effectively within a team. Strong attention to detail, excellent organizational skills, and the ability to prioritize and multitask. Excellent computer skills including Excel, Word, and database experience such as REDCap; demonstrated ability to learn new technologies. Preferred Skills and Abilities Master’s degree in a related field (e.g., public health, social sciences). Experience preparing IRB protocols, amendments, and progress reports. Experience with clinical trials, including patient recruitment and regulatory submissions; experience conducting manualized addiction counseling sessions. Familiarity with statistical analysis software (e.g., SPSS, SAS, R) and experience with REDCap. Prior experience working on large‑scale research studies or multi‑visit projects. Principal Responsibilities Carry out research within the scope of the established study protocol; adhere to all human subjects regulations as defined by Yale University and the federal government. Develop criteria for admission of study subjects based on project goals and objectives. Determine potential sources of funding and prospective partnerships; evaluate feasibility of potential projects. Negotiate contracts and/or changes with funders. Develop original HIC/IRB submissions; collaborate with PIs on revisions and contribute to scientific protocols. Develop forms, questionnaires, and research techniques; write procedures manuals for data collection and coding. Document and transmit study data; ensure accurate and timely completion of report forms at each site. Manage and coordinate multi‑site studies; serve as primary coordinator between university, non‑Yale collaborators, pharmaceutical companies, HIC, IRB, and funding sources. Perform descriptive and multivariate statistical analyses of data using computer software. Design and implement quality control measures to ensure accurate collection and processing of data. Contribute original thought and relevance to written reports; assist in writing abstracts and manuscripts. Required Education and Experience Master’s degree in a related discipline and two years of experience, or an equivalent combination of education and experience. Equal Employment Opportunity Statement University policy is committed to affirmative action under law in employment of women, minority group members, individuals with disabilities, and protected veterans. In accordance with Yale's Policy Against Discrimination and Harassment, Yale does not discriminate against any individual on the basis of sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, or veteran of the Vietnam era. #J-18808-Ljbffr