Psychometric Rater

Evolution Research Group•Fort Myers, FL

4d•Onsite

About The Position

As a Psychometric Rater, you will be responsible for the organization, administration, management, and efficient execution of clinical ratings associated with clinical trials. You will work closely with a team of researchers and clinicians to ensure that all study protocols are followed, and that data is collected in a timely and ethical manner. The Rater works under the direction of the Principal Investigator and the Site Director and maintains accurate and confidential documentation of study participants. In executing these responsibilities, the Rater is guided by FDA regulations, Good Clinical Practice (GCP), relevant workplace practices, and company standard operating procedures.

Requirements

Bachelor’s, RN, or master’s degree required; PhD preferred.
Rater experience required.
Strong attention to detail
Excellent organizational and time management skills
Ability to work independently and as part of a team

Nice To Haves

Master's degree in psychology or related field
Experience working in a research setting
Familiarity with electronic data capture systems
Strong written and verbal communication skills

Responsibilities

Administer and score tests to study participants
Ensure accurate and efficient data collection
Follow study protocols and ethical guidelines
Collaborate with a team of researchers and clinicians
Ensure the applicable license is current and valid.
Obtain detailed knowledge of all components of a study protocol relevant to completion of rating scales through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.
Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.
Manage aspects of the study related to ratings with the rater training representative, study sponsor, Site Director, and Principal Investigator to ensure compliance with protocol requirements.
Assist in recruitment efforts as directed by PI or Site Director
Collect demographic, medical, psychiatric, and medication history during prescreening interviews for the purpose of determining eligibility for clinical trial participation.
Obtain and document subject consent using the prescreen informed consent.