Clinical Research Rater

Company Description Walnut Clinical Research is a dedicated clinical research site focused on advancing medical knowledge and improving patient outcomes through high-quality clinical trials. The organization partners with sponsors, CROs, and healthcare professionals to conduct ethically sound, well-managed studies in a variety of therapeutic areas. Team members collaborate in a structured, compliant environment that prioritizes participant safety, data integrity, and regulatory adherence. Walnut Clinical Research offers opportunities for professional growth while contributing to meaningful work that supports future treatments and therapies.

Role Description The Clinical Research Rater is a part-time, on-site position based in Valley Stream, NY. This role is responsible for administering standardized clinical rating scales, structured interviews, and assessments to study participants in accordance with study protocols and regulatory guidelines. The Clinical Research Rater will document findings accurately, ensure timely completion of case report forms, and collaborate with investigators and coordinators to evaluate participant eligibility and track study progress. Daily responsibilities include maintaining assessment schedules, participating in team meetings, supporting protocol training, and helping ensure data quality and consistency across studies. The role also involves adherence to Good Clinical Practice (GCP), site SOPs, and sponsor requirements while maintaining a professional and respectful environment for all participants.

Qualifications

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• Demonstrated ability to administer and score clinical assessments, rating scales, and structured interviews with attention to detail and consistency.
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• Strong clinical judgment and observational skills to evaluate participant symptoms, behavior, and functional status within defined protocols.
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• Effective written and verbal communication skills for documenting assessments, communicating findings to the study team, and interacting with participants.
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• Solid organizational and time-management skills to manage multiple studies, schedules, and deadlines in a fast-paced clinical research setting.
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• Familiarity with clinical research processes, Good Clinical Practice (GCP), and regulatory requirements; prior experience in clinical trials or behavioral health is preferred.
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• Comfort working with diverse populations and maintaining a patient-centered, professional, and non-judgmental approach.
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• Proficiency in basic computer applications and electronic data capture systems used for research documentation.
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• Master's or Doctorate level degree in psychology, nursing, social work, neuroscience, or a related field; advanced training or certification in clinical rating scales (e.g., psychiatric or neurological scales) is a plus.
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• Ability to work on-site in Valley Stream, NY, with reliable attendance and collaboration as part of a multidisciplinary research team.
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