Clinical Research Associate

Yale Clinical Research OpportunityWorking at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Discover your opportunities at Yale!This individual will be responsible for: implementation of the clinical research operation of the Testani laboratory; will be responsible for working independently and in collaboration with the research team towards recruitment of participants for the research protocols, obtain informed consent, responsible for creation and, maintenance of accurate data records, managing of regulatory compliance in several ongoing heart failure studies in both hospitalized and ambulatory patients work in conjunction with the research team to carry out study procedures and process biospecimen.The research program and laboratory conduct clinical and translational research in the areas of cardio-renal interactions in heart failure. The program maintains a large biorepository and utilizes novel technologies/processes and state-of-the-art instrumentation to carry out high throughput processing.Required Skills and Abilities1. Strong organization skills, attention to detail and the ability to prioritize and multi-task. Prior experience with clinical trials, with demonstrated ability to function as a collaborative member of a clinical research team and communicate well with participants and providers.2. Demonstrated excellence in organizational skills, attention to detail, and ability to multi-task.3. Skilled in obtaining informed consent, proven skill for laboratory sample processing and collecting vital signs.4. Excellent time management skills to manage multiple ongoing projects. Excellent oral and written communication skills. Proven experience with IND studies and managing regulatory documents.5. Flexibility and willingness to learn new skills/adapt to different settings i.e. study specific requirements.Preferred Skills and Abilities1. Master's degree in a related field and three years of related work experience in the same job family or an equivalent combination of experience and education.2. Knowledgeable in Redcap, Epic, OnCore, tele and video consenting and phlebotomy.Principal Responsibilities1. 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.