- $60,000 - $70,000 salary based on CRC experience
- Advance into a Clinical Research Psychometric Rater with all training and credentials
- Work with company that focuses on diversity in their trials
- Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans.
- Patient recruitment, enrollment, scheduling, and consent
- Lab procedures and shipments
- Maintain GCP and follow protocols
- Data management in EDC systems
- Overall coordination of the study
- Learn Psychometric rating skills over time to start doing rating scales
- 1+ year of experience working as a CRC in a non-academic setting
- 1+ year of experience with Sponsor backed clinical trials
- Phlebotomy experience
- Bilingual/fluent in Spanish and English
Clinical Research Coordinator - Plymouth Meeting, United States - Sqrl
Description
Highlights
The Company
Our client is a fast growing site network that currently has 14 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. Right now they are looking to expand their on site team in Plymouth Meeting, MD with an experienced CRC that wants to advance into a Psychometric rater
Responsibilities
As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process
Qualifications: