- Play a major role in advancing medicine with a team dedicated to the patient experience
- Full Benefits for full-time (Health, Dental, Vision, 401k w/ 4% Match, 15 days of PTO, 10 Paid Holidays)
- Competitive compensation
- Gain experience in the fast-growing world of clinical research and develop skills that are in high demand
- Monday - Friday 8:30 AM - 5 PM with some flexibility to meet patient schedules (differs for part-time schedules)
- The company is invested in growth, providing employees with unique opportunities for career advancement
- Join a dedicated team at a large site with opportunities for advancement at the site and site network level.
- Administer clinical efficacy scales on subjects with various diagnoses such as ADHD, Alzheimer's Disease, Bipolar Disorder, Major Depressive Disorder and Substance Use Disorders.
- 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.
- Master's Degree in a related field
- Bilingual (Fluent/Native in English and Spanish)
- 6 months or more of experience in psychometry or handling rating scales in clinical research
- Rater qualification certification preferred
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Clinical Research Rater - Plymouth Meeting, United States - SQRL
Description
Open to part-time or full-time Clinical Ratersaa1
Highlights
Company
Our client is a Clinical Research site network with over 17 research sites across the United States. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, women's health, and vaccines. They are a fast-growing site network with plans to grow from 17 sites to over 30 sites in 2024 alone.
Position
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.
Qualifications
