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 and two years of experience or equivalent combination of education and experience. Experience with disadvantaged populations is a plus. Experience with REDCap or similar software strongly preferred. Prior training on Human Subjects Protection and HIPAA/Privacy. Prior regulatory experience. Fluency in Spanish is a plus.

Preferred Education, Experience and Skills:   Master's degree in biological sciences or public health and two years of experience or equivalent combination of education and experience. Experience with disadvantaged populations is a plus. Experience with REDCap or similar software strongly preferred. Prior training on Human Subjects Protection and HIPAA/Privacy. Prior regulatory experience. Fluency in Spanish is a plus.

Required Skill/ability 5:   Ability to work as part of a team with diverse backgrounds and disciplines. Ability to provide reports on study progress during weekly team meetings.

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.

Work Week:   Standard (M-F equal number of hours per day)

University Job Title:   Research Associate 2, HSS

Required Skill/ability 1:   Experience in recruiting patient participants in a clinic or agency setting and obtaining informed consent.

Required Skill/ability 4:   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.

Required Skill/ability 2:   Excellent interpersonal, verbal, and organizational skills, professionalism, and the ability to function independently. Strong attention to detail as required for data collection and data entry.

Master's Degree in a related discipline and two years of experience or an equivalent combination of education and experience.