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: Ability to work with FDA regulators on an IDE/IND study. Experience in a clinical setting as a clinical technician, RN, and/or clinical research is preferred. Excellent grant-writing skills (prior experience preferred). Understanding and working knowledge of FDA IDE/IND study requirements.
Preferred Education, Experience and Skills: Ability to work with FDA regulators on an IDE/IND study. Experience in a clinical setting as a clinical technician, RN, and/or clinical research is preferred. Excellent grant-writing skills (prior experience preferred). Understanding and working knowledge of FDA IDE/IND study requirements.
Posting Position Title: Research Associate 2, HSS
Required Skill/ability 3: Demonstrated self-motivation, independence, consistency and reliability, including excellent attendance and punctuality. Proven ability to be extremely organized, detailed orientated and a strong communicator.
Work Week: Standard (M-F equal number of hours per day)
University Job Title: Research Associate 2, HSS
Required Skill/ability 1: Proven ability conducting and supporting all phases of research in a clinical environment including data management and analyses. Ability to multi-task in challenging clinical environment (cardiac arrest).
Required Skill/ability 4: Proven ability to effectively, efficiently and independently work under pressure, and to set priorities among multiple competing tasks. Excellent oral/written communication and leadership skills.
Required Skill/ability 2: Ability to coordinate tasks between multiple members of a diverse clinical team at two different enrollment sites (i.e. emergency medicine, vascular surgery, cardiology at Yale and UC Davis).
Master's Degree in a related discipline and two years of experience or an equivalent combination of education and experience.
Internal Number: 53696BR
About Yale University
Yale University is an American private Ivy League research university located in New Haven, Connecticut. Founded in 1701 in the Colony of Connecticut, the university is the third-oldest institution of higher education in the United States.