Psychometric Raters

Job Description

Job Description

At K2 Medical Research, a privately-owned clinical research facility with multiple locations in Florida, Tennessee, and Rhode Island. We specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. Here at K2, we are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world.

K2 is building a talent pipeline for future Psychometric Raters to support a new clinical research initiative in Nashville, TN . This position offers an incredible chance to contribute to advancing our understanding of neurodegenerative diseases, providing valuable experience in both research and patient care. K2 Medical Research is committed to fostering a collaborative and supportive environment, where Psychometric Raters can thrive and make significant contributions to the field.

This is an evergreen requisition , meaning we don't have an immediate opening , but we're actively seeking talented professionals for upcoming opportunities. By applying, your information will be reviewed and considered for future roles as they become available. If you're interested in a future with K2 Medical Research, we encourage you to apply!

Description :

The Psychometric Rater is responsible for administering and interpreting quantitative and qualitative tests as part of a clinical team investigating pharmaceutical treatments for related disease state which include but are not limited to, Alzheimer’s disease, Mild Cognitive Impairment, Depression, Anxiety, and Parkinson’s Disease. This position is responsible for ensuring that the data collection is in congruence with the philosophy and mission of the company, as well as with the specific scale administration guidelines. The Psychometric Rater follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff, sponsoring agencies, and others to effectively perform required testing and related research activities. All duties carried out by the Psychometric Rater are done so in accordance with company policies and SOPs, Good Clinical Practice, as well as all applicable local, state, and federal regulations. Professionals in this role actively participate in outstanding customer service and accept responsibility for developing and maintaining mutually respectful relationships.

Primary Responsibilities :

• Conduct cognitive, diagnostic, and clinical assessments of study participants, as well as caregiver interviews for clinical trials under the direction of a supervising Principal Investigator in accordance with FDA, GCP, and protocol guidelines.
• Actively work to maintain consistency in the performance of ratings over time for individual subjects to ensure efficacy and prevent rater drift.
• Articulate ratings issues to CRO and / or Sponsor, Principal or Sub-Investigator and other members of the study team.
• Maintain accurate, complete, and timely visit source documentation as well as sponsor required information.
• Respond promptly to questions and feedback regarding rating assessments.
• Ensure subject safety by appropriately assessing and responding to any potential for harm to self or others and reporting it appropriately per company policy.
• Facilitate flow of professional and timely communication with subjects, study staff, referral sources, Sponsor and / or CRO, Monitor(s), Auditors and any central rating organizations hired by the Sponsor.
• Complete all study queries in a timely manner.
• Administering and scoring psychometric tests for clinical trial participants in accordance with the visit schedule outlined in the study protocol.
• Maintain compliance with all company policies and procedures.
• Provide appropriate community resource referrals to subjects, caretakers, and family, as appropriate. Assist with additional tasks as assigned.
• Conduct telephone screens and pre-screens, as needed.
• Supervise study lead duties over 4 studies at minimum.
• Complete weekly schedule check supervising a minimum of 2 coordinators.
• Administer protocol-specific scales and evaluate results to determine protocol eligibility under the supervision of the Principal Investigator.

Knowledge, Skills, and Abilities :

Qualifications :

Benefits :

We value our employees and their professional and personal needs, and support these through our benefit offerings :

Join the K2 Family : Where Compassion and Connection Lead the Way!

At K2 Med, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff. We thrive on empathy, a patient-first approach, and absolutely zero big egos (unless it's an ego about being extra kind, then we'll allow it!). We believe a supportive, caring experience is paramount for our patients, and that starts with you.

We celebrate what makes you uniquely you! Your race, color, religion, marital status, age, national origin, or even your favorite snack (though we're partial to good research snacks) don't define your talent or fit here. If you need a little extra support or accommodation due to a disability, no sweat! Just reach out to our friendly team at HR@k2med.com, and we'll ensure you have everything you need to shine.