Neuropsychologist (Clinical Research)

SQRL

Chicago (IL)

On-site

USD 90,000 - 110,000

Full time

14 days+

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Benefits offered by this job

401k with match

15 days PTO

Medical insurance

Vision insurance

Paid maternity leave

Disability insurance

Job summary

A reputable clinical research organization in Chicago is seeking an Associate Director of Recruiting. This role involves working closely with Principal Investigators on various clinical research trials and administering psychometric tests to study participants. A PsyD degree is required, and candidates should have a passion for clinical research, with the ability to work onsite. The position offers a salary of $90,000 - $110,000 and great benefits, including 401k matching and paid time off.

Qualifications

Excitement to work within the Clinical Research Field.
Ability to work on site in Chicago.

Responsibilities

Administer various psychometric efficacy scales and interviews on study participants.
Work hand in hand with the Principal Investigator on clinical research trials.
Determine eligibility for research trials.

Skills

Clinical Research

Psychometric evaluations

Communication with Study Monitors

Education

PsyD Degree

Job description

3 days ago Be among the first 25 applicants

This range is provided by SQRL. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Associate Director of Recruiting at SQRL | Clinical Research, Healthcare, Biotech, Life Sciences

Highlights

$90,000 - $110,000 salary based on experience
Great benefits including 401k w/match and 15 days PTO
Play a significant role in the research for new therapies
Work with a company that truly cares about their employees and patients

About Our Client

Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.

Responsibilities

You will be responsible for administering various psychometric efficacy scales and completing interviews/ratings on study participants specific to several study protocols to determine current levels of functioning and to create a clinical impression of the study subject’s current presentation throughout the duration of the trials.

Work hand in hand with the Principal Investigator on a variety of clincal research trials
Administer clinical efficacy scales on subjects with various diagnoses such as Parkinson's, Alzheimer’s Disease, Bipolar Disorder, Major Depressive Disorder
Perform diagnostic evaluations
Determine eligibility for research trials
Work with Principal Investigators and coordinators in initiating assessments and data query completion and data clarification
Interact with Sponsors, Study Monitors and Medical Monitors from pharmaceutical companies in a professional manner.

Qualifications