Clinical Cognitive Rater for Alzheimer's Trials

ADP, Inc.; San Antonio (TX); On-site; USD 60,000 - 80,000; Full time

Job summary

ADP, Inc. in San Antonio, TX seeks a Psychometric Rater to measure cognitive and behavioral function in Alzheimer's disease trials. You will administer standardized tests and ensure data accuracy while coordinating with clinical staff, sponsors, and participants.

The role emphasizes adherence to GCP/IRB, data integrity, and ongoing training within a multidisciplinary team in a full-time setting.

Qualifications

• Bachelor's degree in social work, psychology or related health field; master's preferred.
• Experience with geriatric populations and multidisciplinary teams required.
• Proficient in administering cognitive assessments; research experience preferred.

Responsibilities

• Administer assessments for the Free Memory Screen Clinic.
• Administer cognitive tests and rating scales.
• Maintain scales, address queries, complete training.
• Serve as a rater on AD, MCI, and PD trials.
• Aid in recruitment databases and outreach for trials.
• Participate in meetings and QA activities.
• Ensure data are recorded accurately in the study database.
• Adhere to GCP and IRB requirements; protect participant data.
• Stay current with protocol updates and training.
• Collaborate with Principal Investigator and clinical staff.

Skills

Excellent written and oral comms

Spanish proficiency

Organizational skills

Attention to detail

People skills

Flexibility with priorities

Diplomatic communication

Report and presentation skills

Interpersonal skills

Mathematical knowledge

Microsoft Office

Web-based enterprise software

Education

Bachelor's in social work, psychology or related health field

Masters in relevant areas preferred

Tools

Microsoft Office

Web-based enterprise solutions software

Job description

ADP, Inc. in San Antonio, TX seeks a Psychometric Rater to measure cognitive and behavioral function in Alzheimer's disease trials. You will administer standardized tests and ensure data accuracy while coordinating with clinical staff, sponsors, and participants.

The role emphasizes adherence to GCP/IRB, data integrity, and ongoing training within a multidisciplinary team in a full-time setting.