Psychometric Specialist

Adecco • Wilmington, NC

402d • $93,600 - $110,240 • Remote

About The Position

The Psychometric Specialist will play a crucial role in advancing healthcare solutions by administering and interpreting quantitative tests related to psychological variables associated with various diseases and disorders. This position involves working closely with clinical trials, ensuring data collection aligns with company guidelines, and maintaining communication with sponsors and site staff. The role requires expertise in psychometric ratings, training, and adherence to regulatory standards.

Requirements

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
• Publications experience demonstrating expertise in instrument development, including reliability, validity, responsiveness, and meaningful within-patient change.
• Ability to write psychometric statistical analyses plans or clinical trial PRO endpoint analyses SAPs.
• Evaluates COAs for appropriate usage in clinical trials, including acceptability to FDA guidelines.
• Develops analysis plans and guides them through the development of regulatory dossiers for COAs.
• Advanced computer skills, including proficiency with Microsoft Office and capability to learn new software/hardware.
• Strong oral and written communication skills, including the use of Business English.
• Ability to work independently or in a team environment.
• Strong attention to detail and strong problem-solving abilities.
• Skilled in all types of audit preparations and oversight during audits.
• In-depth industry knowledge of quality compliance and GCP regulations.

Responsibilities

• Administers and interprets quantitative tests for measuring psychological variables related to diseases and disorders.
• Completes psychometric ratings for clinical trial performance at the site level.
• Administers psychometric ratings for clinical trials under the supervision of a Principal Investigator.
• Facilitates study-specific Psychometric Rater training for new and ongoing studies.
• Maintains ongoing communication with sponsors and site staff regarding ratings-related protocol updates.
• Identifies potential problems or inconsistencies and takes appropriate action.
• Administers and interprets protocol-specific scales to determine protocol eligibility.
• Ensures subject safety by responding appropriately to any potential harm identified during interviews and evaluations.
• Maintains consistency in the performance of ratings for individual subjects and clinical trials.
• Maintains timely source documentation and sponsor-required information.
• Completes all monitor and sponsor queries promptly.
• Provides educational in-services for third-party vendors providing protocol-specific care to subjects.
• Ensures adherence to COPs, SOPs, and GCP regulations.

Benefits

• Medical insurance
• Dental insurance
• Vision insurance
• Life insurance
• Short-term disability
• Additional voluntary benefits
• EAP program
• Commuter benefits
• 401K plan
• Paid Sick Leave
• Holiday pay

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Administrative and Support Services
• Education Level: Bachelor's degree