1. Carries out research within the scope of the established study protocol. Adheres to all human subjects regulations as defined by Yale University and the federal government that pertain to research studies. 2. Develops criteria for admission of study subjects based on goals and objectives of project. 3. Determines potential sources of funding and prospective partnerships. 4. Evaluates feasibility of accepting potential projects through analysis of staffing needs, resource requirements, financial costs, and current planned capacity of group. Negotiates contracts and/or changes with funder. 5. Develops original HIC/IRB submissions.  Based on knowledge of science and research goals, collaborates with PIs on major revisions and contributes to scientific protocols.  Plans and implements changes. 6. Develops forms, questionnaires and the application of research techniques; writes procedures manuals for data collection and coding. 7. Responsible for the documentation and transmission of study data.  Ensures that report forms are accurately documented and completed in a timely manner at each site location. 8. Works independently to develop manage and organize multi site studies.  Serves as primary coordinator between University, non-Yale collaborators, pharmaceutical companies, HIC, IRB and funding sources. 9. Performs descriptive and multivariate statistical analyses of data, using computer software. 10. Designs and implements quality control measures to ensure accurate collection and processing of data. 11. Contributes in-depth, original thought and relevance to written reports and to the writing of abstracts and manuscripts.

Preferred Education:  Master's degree in biological sciences or public health. Prior work with patients with opioid use disorder and chronic pain. Experience with disadvantaged populations. Experience with REDCap or similar software strongly preferred. Prior training on Human Subjects Protection and HIPAA/Privacy. Prior regulatory experience. Fluency in Spanish.

Preferred Education, Experience and Skills:  Master's degree in biological sciences or public health. Prior work with patients with opioid use disorder and chronic pain. Experience with disadvantaged populations. Experience with REDCap or similar software strongly preferred. Prior training on Human Subjects Protection and HIPAA/Privacy. Prior regulatory experience. Fluency in Spanish.

Required Skill/ability 5:  Experience with electronic medical records. Proficiency with Microsoft Office (Outlook, Word, Excel.) Knowledge of medical terminology. Ability to obtain relevant health information, such as pharmacy data. 

Posting Position Title:  Research Associate 2, HSS

Required Skill/ability 3:  

Ability to work with people of diverse backgrounds. Ability to work independently with minimal supervision and highly motivated.