
Psychotherapist Rater
Join the Centricity Research Team!
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
Psychotherapist Clinical Rater– PTSD Clinical Trial
About the Role
We’re looking for an experienced, trauma-informed clinician to join our team on a casual basis as a Primary Support Provider for an upcoming clinical trial in post-traumatic stress disorder (PTSD). In this role, you’ll administer standardized psychiatric and cognitive assessments to study participants – including the CAPS-5, the gold-standard clinical interview for PTSD – producing reliable, protocol-compliant ratings that serve as key study endpoints.
Working closely with the Principal Investigator and study team, you’ll bring sound clinical judgment, a calm and neutral interviewing style, and a strong commitment to participant safety, confidentiality, and study integrity. This is a great opportunity for clinicians who want to contribute to innovative mental health research on a flexible, study-based schedule.
What You’ll Do
- Administer and score the study rating scales you are approved for, which may include the CAPS-5 (Clinician-Administered PTSD Scale for DSM-5), M.I.N.I. (diagnostic interview), CGI-S (illness severity), BPRS+ (psychiatric symptoms), E-TRIP-S, and WAIS-IV Digit Symbol Substitution Test (DSST).
- Conduct screening interviews to confirm diagnosis and eligibility, and repeat assessments at scheduled follow-up visits.
- Follow each scale’s standardized administration and scoring conventions exactly to keep ratings consistent across visits and raters.
- Complete sponsor-required rater training and scale certification before rating any participant, and take part in calibration exercises, recertification, and audio/video review of interviews as required.
- Maintain blinding and independence as required by the study protocol.
- Record ratings accurately in source documents and EDC within protocol timelines, following ALCOA+ principles.
- Resolve data queries and support monitoring visits and audits.
- Recognize and immediately escalate suicidality, acute distress, or other safety concerns to the investigator.
You Might Be a Great Fit If You:
- Hold an MD, DO, doctoral or master’s degree in psychiatry, psychology, or a related field, or are an APRN, NP, PA, or RN with a BSN (internationally equivalent education is accepted).
- Have at least 2 years of clinical experience working with people with PTSD.
- Have experience administering structured clinical assessments – hands-on experience with the CAPS-5, M.I.N.I., SCID, BPRS, or DSST is a strong asset.
- Bring prior clinical trial rating experience, ideally in PTSD, depression, or psychedelic-assisted therapy studies (an asset).
- Hold GCP certification, or are willing to obtain it.
- Have strong, trauma-informed interviewing skills and a calm, neutral manner.
- Are consistent and detail-oriented, with a commitment to accurate, timely documentation.
- Exercise discretion in maintaining blinding and participant confidentiality.
- Are willing to complete sponsor rater training and certification, and have availability for scheduled study visits on a casual basis.
Role Details
Compensation: $125–$150 CAD per hour, based on relevant clinical experience, PTSD assessment expertise, and clinical-trial rater experience.
Employment type: Casual. Hours vary according to study requirements and participant scheduling; no minimum hours are guaranteed.
Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
- Quality: We aim for excellence and integrity in everything we do - because lives depend on it.
- Care: We show up for each other, our customers, and our mission - always going the extra mile.
- Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
- One Team: We collaborate, support one another, and succeed together.
- Grow for Good: We grow with purpose - to expand access to research and improve global health.
- Own It: We take initiative, deliver results, and follow through - with passion and accountability.
Ready to Apply?
We’d love to hear from you – apply now!
We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.
Clinical Operations
Toronto, Canada
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