Clinical Research Coordinator 1

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Overview

The Research Associate I will support clinical research in the Ranganathan Research Lab at the intersection of psychiatry, neuroscience, and substance use. The position will contribute to studies examining psychiatric disorders, including schizophrenia and depression, and research involving cannabis, cannabinoids, ketamine, and other novel therapeutic approaches. Responsibilities include coordinating day-to-day research activities; assisting with participant recruitment, screening, scheduling, informed consent, and study visits; collecting, entering, managing, and reviewing research data; maintaining study documentation and regulatory files; supporting IRB submissions, amendments, continuing reviews, and other regulatory requirements; assisting with biospecimen and/or neurobehavioral research procedures as applicable; conducting literature reviews and contributing to data analyses and development of reports, presentations, and manuscripts; and collaborating with investigators, clinicians, research staff, and external partners. The Research Associate will help ensure that studies are conducted accurately, efficiently, and in accordance with approved protocols, institutional policies, and human subjects research requirements. They will demonstrate independent decision making by identifying issues, evaluating the available information (e.g. regulatory guidelines), and implementing appropriate solutions within the scope of the role.

Required Skills and Abilities

1. Strong organizational and project-management skills, with the ability to coordinate multiple research studies, priorities, deadlines, and study documents with close attention to detail.

2. Demonstrated ability to support human subjects research, including participant recruitment, screening, scheduling, informed consent, study visits, and professional communication with research participants.

3. Proven experience with clinical research regulatory and compliance activities, including preparation and maintenance of IRB submissions, amendments, study binders/files, and protocol documentation.

4. Proficiency with research data collection, entry, quality review, database management, and basic data analysis; ability to maintain accurate, confidential records and ability to work with REDCap or comparable systems.

5. Excellent written, verbal, and interpersonal communication skills, prepare reports and presentations, and collaborate effectively with multidisciplinary research teams.

Preferred Skills and Abilities

1. Master's-level coursework or degree in public health, psychology, neuroscience, or a related field preferred.

2. Proven experience in psychiatric, neuroscience, substance use, or clinical research.

3. Proven experience with IRB/regulatory submissions, participant recruitment and screening, informed consent, REDCap or similar research databases, and preparation of research reports or presentations.

4. Familiarity with EEG, VR, biospecimen workflows, or other clinical research technologies is a plus.

5. Strong interest in translational mental health research and the development of novel biomarkers and treatments.

Principal Responsibilities

1. Serves as the primary oversight specialist on clinical and operational processes for low to moderately complex studies and non-therapeutic trials. Serves as a supporting clinical research coordinator to CRC/CRN II and Sr. CRC/CRN for highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, completion, and administration for low to moderately complex studies and non-therapeutic trials. 3. Contributes to study feasibility reviews and makes recommendations based on analysis of the protocol and knowledge of clinical trials, operations, and ICH/GCP, federal regulation, and institutional processes for low to moderately complex clinical trials and non-therapeutic trials. 4. Ensures low to moderately complex study protocols are adhered to, oversees the maintenance of accurate documentation, recruitment of study participants and ensures regulatory and protocol requirements and guidelines are met per ICH/GCP, federal regulation, and institutional and sponsor requirements. 5. Identifies instances of noncompliance and deviations from protocol and works with manager to analyze and advises noncompliance and deviations to the appropriate parties. 6. Advises Principal Investigator oversight on low to moderately complex clinical trials and non-therapeutic trials by providing updates on protocol issues, status of signatures and clinical significance on lab reports, ECGs, adverse events and other documents as required. 7. Analyses, documents and conveys study data on low to moderately complex clinical trials and non-therapeutic trials. Coordinates with assigned staff to oversee and ensure that report forms are accurately documented and completed in a timely manner. 8. Oversees the tracking and reporting of adverse events, serious adverse events, protocol waivers, deviations, and violations on low to moderately complex clinical trials and non-therapeutic trials. 9. Assesses trial execution for assigned low to moderately complex trials and non-therapeutic trials and identifies areas that need improvement or that require correction and provides education and/or recommendations, as needed. 10. Collaborates with Investigators and Research Managers in the preparation and execution of corrective and preventative action plans and ensures implementation and adherence to stated plan for low to moderately complex trials and non-therapeutic trials. 11. Collaborates with the Quality Education Unit to contribute to the design of CRC trainings and continuing education. 12. Participates in interim monitoring visits and internal audits. 13. Monitors, interprets, and communicates federal and state regulations, and local policies for new guidance, updates, or policies. 14. Performs other duties as assigned. Required Education and Experience Bachelor's degree in a health-related discipline, or other related field and one (1) year of clinical research experience, or the equivalent combination of education or experience. Knowledge of Good Clinical Practices (GCP) and Federal Regulations is required. Experience must indicate the ability to work with minimal supervision in a team environment. Required License(s) or Certification(s) Required License(s) or Certification(s): Physical Requirements Physical Requirements:

Job Posting Date

10/23/2026

Job Category

Professional

Bargaining Unit

NON

Compensation Grade

Administration & Operations

Compensation Grade Profile

Supervisor; Senior Associate (22)

Salary Range

$61,500.00 - $91,875.00

Benefits

A general description of the benefits to be offered with this Managerial & Professional position is available at:

Yale Benefits

Time Type

Full time

Duration Type

Staff

Work Model

On-site

Background 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.

The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-related duties through their hiring department.

The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its faculty, staff, and student body qualified persons from a broad range of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual's sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.

Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).

Note

Yale University is a tobacco-free campus.