"Research Associate I"

Overview

The Research Associate will manage and provide statistical analysis support for multi-faceted translational research projects operated through the Stress Center in the Department of Psychiatry. This position will serve as the primary interface between the data collection and data management and monitoring and analysis for ongoing studies in stress, alcohol and substance use disorders. With a high degree of independence, the research associate will coordinate with University, YCCI, IRB and other regulatory departments as well as collaborating research laboratories to successfully organize, monitor, assess and analyze multi-level subjective, biological, cognitive, and clinical outcome data. Responsibilities will include research project management and monitoring of protocols, IRB amendments and protocol development, FDA/IND, data management, statistical analysis, report preparation, manuscripts and grant writing support. The research associate will assist in development, implementation and maintenance of original research protocols and the related quality assurance and study monitoring procedures as well as preparation of manuscripts, presentations and publications.

Required Skills and Abilities

1. Knowledge and expertise in statistical analyses for psychology/psychiatry and packages such as R Studio, SAS/SPSS, AMOS, and ability to perform statistical analyses.
2. Solid knowledge of clinical research protocols, and implementation of data management and monitoring for protocols and data cleaning and organization strategies for successful and efficient processing of multiple streams of data. Additional computer skills including Excel, Word, Power point, Endnote reference manage, REDCAP and demonstrated ability to learn new technologies.
3. Excellent oral and written communication skills. Ability to interact with successfully with staff and faculty and function independently as well as function effectively within a team in an academic environment.
4. Ability to work independently as well as function effectively within a team.
5. Strong attention to detail, excellent organizational skills, and the ability to prioritize and multitask.

Preferred Skills and Abilities

Experience with patient related clinical research.

Principal Responsibilities

1. Recommends the design and implementation of procedures and protocols under the direction of a higher-level authority.
2. Investigates, analyzes, and reaches preliminary scientific conclusions related to research planning
3. Ensures data results are compiled, analyzed, and presented properly.
4. Analyzes, develops and interprets scientific results. Maintains clear documentation of results. Prepares scientific reports and papers for research proposals and published reports.
5. Performs independent research and laboratory techniques and participates in experimental research planning.
6. Interacts with internal contacts including the PI, research assistants, graduate students, Radiation Safety and Biological Safety officers, and Animal Care personnel to discuss and evaluate research results and to ensure the smooth and safe operation of the laboratory.
7. Interacts with external contacts such as researchers at other institutions, staff at biotechnology and reagents companies to consult on research methods and to keep abreast of product information and developments.
8. May perform other duties as assigned.

Required Education and Experience

Master’s Degree in a scientific discipline and one year experience or an equivalent combination of education and experience.