Clinical Laboratory Scientist

RWD Consulting•Silver Springs, MD

3d•Onsite

About The Position

This position involves evaluating protocols for compliance with regulations governing human subjects' protection, providing oversight for an "honest broker" system, and coordinating the functions of auxiliary departments on proposed studies. The role includes participating with the Principal Investigator in the scientific design of protocols, making recommendations on methodology, and ensuring proper documentation of projects, with a focus on protocol modifications.

Requirements

BS, RN or BSN degree or equivalent
2-5 years of experience in the field or in a related area
Professional knowledge of a wide range of scientific and biomedical concepts, principles and practices to perform the highly specialized tasks of developing and supporting proposed and active clinical cases
Interpreting regulations associated with the studies and identifying potential threats to compliance with regulations and requirements in clinical settings
Ability to communicate with physicians and other healthcare personnel in a professional capacity
Working knowledge of a significant body of scientific, biomedical concepts and terminology and medical concepts and terminology

Responsibilities

Evaluates protocols for compliance with applicable regulations governing human subjects’ protection.
Provides oversight and coordinates the functions associated with an “honest broker” system.
Analyzes the role and impact of other auxiliary departments on the proposed studies and coordinates their input.
Participates with the Principal Investigator in the scientific design of protocols associated with studies and makes recommendations on methodology.
Assures the proper documentation of project/study, giving particular attention to any protocol modifications.