Clinical Research Associate

4 days ago

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TFS HealthScience

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CRO • clinical trials • Scientific and Medical consulting • Contract Placement Solutions (staffing) • Regulatory Consulting

501 - 1000

Description

• Responsible for initiation, monitoring, and termination of investigative sites • Travel as needed, may involve overnight and international travel • Monitor clinical trials in accordance with regulations and guidelines • Review CRFs and subject source documentation for accuracy • Identify site problems and initiate corrective actions

Requirements

• Bachelor’s Degree, preferably in life science or nursing; or equivalent • Minimum 1-3 years of relevant clinical experience • Able to work in a fast paced environment with changing priorities • Understand basic medical terminology and science associated with the assigned drugs and therapeutic areas • Possess the understanding of Good Clinical Practice regulations, ICH guidelines

Benefits

• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth