Senior Clinical Research Associate - Oncology

3 days ago

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Catalyst Clinical Research

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Listen, Devise, Breakthrough

Clinical Operations Services • Clinical Resourcing/Staffing • Clinical Teams • Functional Service Provider

201 - 500

Description

• Monitor clinical trial programs and manage regional clinical trial sites. • Collaborate with assigned clinical research team for site selection and audit responses. • Travels up to 80% within assigned territory; conducts site evaluations and study initiations. • Partners with clinical project team; assists with FDA submission preparations. • Maintain a home office if working remotely; manage work activities for budget and timelines.

Requirements

• Bachelor’s degree in a science or health-related discipline or equivalent of 7 years industry experience. • Minimum of 5 years’ experience in clinical research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent oncology clinical trial experience. • Strong knowledge of clinical trial monitoring, regulatory compliance, clinical research methodology and all applicable regulations and guidelines. • Strong organizational and time management skills and the ability to work independently. • Excellent communication and interpersonal skills. • Flexibility and ability to travel routinely to meet project requirements. • Strong knowledge of standard computer applications. • Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa.