Clinical Rater

Green Life Science; Town of Texas (WI); On-site; USD 65,000 - 95,000; Full time

Job summary

Green Life Science seeks an experienced Psychometric Rater to support Phase I–IV clinical trials. You will administer and score clinical rating scales, support participant assessments, and ensure accurate, protocol-compliant data collection in collaboration with Principal Investigators, Site Directors, clinicians and research teams across trials.

The role requires meticulous documentation, independence within a clinical research team, and strong communication to liaise with sponsors.

Qualifications

• Bachelor's, RN or Master's degree required; PhD preferred.
• Previous clinical-trial psychometric rater experience is required.
• Experience administering and scoring validated clinical rating scales.
• Strong attention to detail and accurate documentation skills.
• Excellent organisation and time management.
• Ability to work independently and collaboratively within a clinical research team.
• Strong written and verbal communication skills.

Responsibilities

• Administer and score clinical and psychometric rating scales in accordance with study protocols.
• Complete accurate and timely clinical assessments and documentation.
• Conduct participant prescreening, including demographic, medical, psychiatric and medication history.
• Support assessment of participant eligibility in line with protocol requirements.
• Complete study-specific rater training and maintain competency.
• Work closely with the Principal Investigator and Site Director to ensure rating activities are conducted appropriately.
• Maintain accurate, confidential and audit-ready participant documentation.
• Ensure compliance with GCP, FDA regulations, study protocols and company SOPs.
• Liaise with sponsors and study teams regarding rating requirements and study-specific expectations.
• Support participant recruitment and informed consent activities as required.
• Maintain all applicable professional licences and certifications.

Skills

Clinical-trial experience

Attention to detail

Organization & time management

Written & verbal communication

Independence & teamwork

Education

Bachelor's RN or Master's degree

PhD preferred

Tools

Electronic Data Capture (EDC) systems

Job description

We are looking for an experienced Psychometric Rater to support the delivery of Phase I-IV clinical trials within a leading clinical research organisation.

You will be responsible for administering and scoring clinical rating scales, supporting participant assessments, and ensuring accurate, timely and protocol-compliant data collection. You will work closely with Principal Investigators, Site Directors, clinicians and research teams across clinical trials.

Key Responsibilities

• Administer and score clinical and psychometric rating scales in accordance with study protocols.
• Complete accurate and timely clinical assessments and documentation.
• Conduct participant prescreening, including demographic, medical, psychiatric and medication history.
• Support assessment of participant eligibility in line with protocol requirements.
• Complete study-specific rater training and maintain competency throughout the study.
• Work closely with the Principal Investigator and Site Director to ensure rating activities are conducted appropriately.
• Maintain accurate, confidential and audit-ready participant documentation.
• Ensure compliance with GCP, FDA regulations, study protocols and company SOPs.
• Liaise with sponsors and study teams regarding rating requirements and study-specific expectations.
• Support participant recruitment and informed consent activities as required.
• Maintain all applicable professional licences and certifications.

Requirements

• Bachelor's, RN or Master's degree required; PhD preferred.
• Previous clinical-trial psychometric rater experience is required.
• Experience administering and scoring validated clinical rating scales.
• Strong attention to detail and accurate documentation skills.
• Excellent organisation and time management.
• Ability to work independently and collaboratively within a clinical research team.
• Strong written and verbal communication skills.

Preferred

• Master’s degree in Psychology or a related discipline.
• Experience within a clinical research/site environment.
• Experience in psychiatry, neuroscience, neurology or other CNS-focused trials.
• Familiarity with electronic data capture (EDC) systems.
• Previous sponsor-specific rater training or certification.