Psychometric Rater

Pinnacle Clinical Research- A Summit Solution; Edinburg (TX); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

Pinnacle Clinical Research- A Summit Solution is seeking a Psychometric Rater for Alzheimer’s disease trials. The role focuses on standardized, quantitative testing to measure cognitive and behavioral functioning and to manage psychometric aspects of studies.

The position requires administering cognitive assessments, maintaining scales, and ensuring consistent data collection while complying with GCP/IRB guidelines. Travel to affiliated sites may be involved.

Qualifications

• Bachelor’s in social work, psychology or related health field. Masters in relevant areas preferred.
• Combination of education and significant experience may be considered
• Experience working with a geriatric population
• Ability to work well with a multidisciplinary team as well as independently
• Proficient in administering cognitive assessments
• Research experience preferred

Responsabilités

• Works with affiliates or collaborating research sites
• Administer assessments for the Free Memory Screen Clinic
• Administer cognitive tests and rating scales
• Responsible for the maintenance of the scales such as addressing queries, completing training, etc.
• Serve as a rater on clinical trials for neurodegenerative diseases, especially Alzheimer’s disease, Mild Cognitive Impairment, and Parkinson’s disease
• Aid in management of recruitment databases, conduct recruitment and outreach initiatives for the various clinical trials
• Participate in meetings
• Ensure assessments are conducted consistently and accurately across all participants
• Ensure all data is accurately recorded into the study database
• Maintain confidential and secure handling of all participant data
• Regularly review data for completeness and accuracy and resolve any discrepancies
• Adhere to all regulatory and ethical guidelines, including Good Clinical Practice (GCP) and institutional review board (IRB) requirements
• Participate in quality assurance activities to ensure the integrity of data collection and reporting
• Attend regular training sessions to stay current with best practices and protocol updates
• Work closely with the Principal Investigator, clinical trial coordinators, and other team members to ensure seamless study operations
• Participate in professional development opportunities to enhance skills and knowledge relevant to the role

Description du poste

Summary:

PCR seeks a Psychometric Rater in Alzheimer’s Disease (AD) trials who specializes in the objective measurement of cognitive and behavioral functioning. A psychometric rater will focus heavily on standardized, structured, and quantitative testing batteries. Psychometric raters will be responsible for managing the psychometric aspects of clinical trials, following study-specific protocol requirements and communicating with clinical staff, study sponsor and participants.

Duties and Responsibilities:

• Works with affiliates or collaborating research sites
• Administer assessments for the Free Memory Screen Clinic
• Administer cognitive tests and rating scales
• Responsible for the maintenance of the scales such as addressing queries, completing training, etc.
• Serve as a rater on clinical trials for neurodegenerative diseases, especially Alzheimer’s disease, Mild Cognitive Impairment, and Parkinson’s disease
• Aid in management of recruitment databases, conduct recruitment and outreach initiatives for the various clinical trials
• Participate in meetings
• Ensure assessments are conducted consistently and accurately across all participants
• Ensure all data is accurately recorded into the study database
• Maintain confidential and secure handling of all participant data
• Regularly review data for completeness and accuracy and resolve any discrepancies
• Adhere to all regulatory and ethical guidelines, including Good Clinical Practice (GCP) and institutional review board (IRB) requirements
• Participate in quality assurance activities to ensure the integrity of data collection and reporting
• Attend regular training sessions to stay current with best practices and protocol updates
• Work closely with the Principal Investigator, clinical trial coordinators, and other team members to ensure seamless study operations
• Participate in professional development opportunities to enhance skills and knowledge relevant to the role

Duties, responsibilities, and activities may change, or new ones may be assigned at any time.

Qualifications:

• Bachelor’s in social work, psychology or related health field. Masters in relevant areas preferred.
• Combination of education and significant experience may be considered
• Experience working with a geriatric population
• Ability to work well with a multidisciplinary team as well as independently
• Proficient in administering cognitive assessments
• Research experience preferred

Knowledge, Skills, and Other Abilities:

• Excellent written and oral communication skills
• Proficiency in Spanish preferred
• Organizational skills
• Ability to pay attention to detail
• People skills including possessing a positive, friendly, and professional demeanor
• Ability to be flexible with changing priorities
• Ability to communicate in a diplomatic and professional manner
• Excellent ability to report and present skills
• Strong interpersonal skills
• Strong mathematical knowledge
• Knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software.

Certificates and Licenses:

Valid Driver’s License

FLSA Classification:

This is an exempt position

Work Environment and Physical Demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this role. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Work is performed in an office and/or clinical environment.
• Occasional domestic and/or international travel may be required.
• Ability to work in an upright and/or stationary position for 6–10 hours per day.
• Frequent mobility required.
• Occasionally squatting, kneeling, or bending.
• Light to moderate lifting and carrying (or otherwise moves) objects with a maximum lift of 20–50 lbs.