Clinical Research Analyst
Yale University
| Working 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! Overview Clinical Research Analyst The Clinical Research Analyst will contribute to a diverse portfolio of clinical research activities spanning study development, regulatory coordination, data acquisition, patient-facing research operations, and scholarly dissemination. This role is designed for a highly motivated individual seeking intensive exposure to translational and patient-oriented clinical research in an academic medical setting. The analyst will develop experience in the design, implementation, and coordination of clinical research protocols, including support for prospective clinical studies and clinical trials. Responsibilities will include regulatory document preparation and Institutional Review Board (IRB) submissions, maintenance of study compliance, detailed medical record review and abstraction, and direct interaction with research participants in accordance with established study protocols. Training in Human Subjects Research, HIPAA compliance, and Good Clinical Practice (GCP) will be provided and applied in the context of active clinical research. In addition, the analyst will receive specialized exposure to advanced physiologic monitoring methods, including cerebral oxygenation monitoring and contemporary hemodynamic and blood pressure monitoring platforms. The role will also involve participation in data organization, interpretation, and presentation, with opportunities to assist in the preparation of scientific manuscripts, abstracts, and conference presentations. This position is particularly well suited for recent graduates or early-career professionals seeking rigorous, hands-on experience in clinical investigation prior to graduate or professional training in medicine, public health, neuroscience, or related health professions. Mentorship and Professional Development The Clinical Research Analyst will receive close mentorship through direct collaboration with senior laboratory personnel, participation in weekly laboratory meetings, and regular one-on-one meetings with Dr. Lyman. Additional academic and professional development opportunities may arise through interdisciplinary collaborations within the Department of Neurology and with investigators at partnering institutions. The role is intended to provide not only technical research experience, but also meaningful exposure to the intellectual, operational, and collaborative dimensions of academic clinical research. Successful candidates will demonstrate strong analytical reasoning, intellectual curiosity, and the ability to engage thoughtfully with complex research questions. They should be highly organized, dependable, and capable of managing multiple responsibilities with attention to detail. Strong interpersonal, written, and verbal communication skills are essential, as is the ability to work both independently and collaboratively in a fast-paced academic research environment. Required Skills and Abilities 1. Clinical or Research Environment Experience: Ability to work well in clinical or research settings with a working knowledge of medical terminology and prior experience supporting research studies. Preferred Skills and Abilities 1. Prior research experience, preferably in a clinical, translational, or laboratory-based setting. Principal Responsibilities 1. Works closely with investigators and other study team members including the project manager, for projects or programs of a small size or sections of medium projects and programs to consult, conduct analysis, and identify trial objectives and requirements within specific parameters. 2. Interprets research business needs and translates them into application and operational requirements for a specific area(s) of research. Develops necessary tools and workshops to successfully elicit requirements. 3. Critically evaluates information gathered from multiple sources - research protocols, clinical trial agreements, financial budgets and fees associated with research - to reconcile conflicts, and decompose high-level information into data essentials. 4. Analyzes data with standard methods, interprets the results, and provides written summary and reporting of data analysis. Develops reporting modules, ad-hoc reports and related reporting tools. Conducts research, data analysis, modeling, projecting and scenario analyses, with the aid of planning technology and databases 5. Develops and maintain documentation and libraries on key processes. 6. Assesses risk and ensures compliance with research protocols/guidelines, university procedures, and third party regulations. 7. Determines training needs, designs, develops and conducts training sessions, meetings and conference calls with study teams and staff members. 8. Performs or assists with research compliance audits or self-assessments. 9. Communicates effectively the perspective of business opportunities, needs, and risks.Required Education and Experience Bachelor’s degree in a related field and one year of related work experience in the same job family or an equivalent combination of experience and education. Must be knowledgeable in regional and federal regulations with the ability to perform independent decision-making on a daily basis. Job Posting Date 04/30/2026Job Category ProfessionalBargaining Unit NONCompensation Grade Administration & OperationsCompensation Grade Profile Supervisor; Senior Associate (21)Salary Range $55,000.00 - $85,000.00Time Type Full timeDuration Type Staff Fixed Duration (Fixed Term)Work Model HybridBackground Check Requirements All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website. Health Requirements Certain positions have associated health requirements based on specific job responsibilities. These may include vaccinations, tests, or examinations, as required by law, regulation, or university policy. Posting Disclaimer Salary offers are determined by a candidate’s qualifications, experience, skills, and education in relation to the position requirements, along with the role’s grade profile and current internal and external market conditions.
Note Yale University is a tobacco-free campus.
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