Senior Clinical Research Associate - Oncology

September 26

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Catalyst Clinical Research

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

201 - 500

Description

• Monitor clinical trial programs and manage regional clinical trial sites. • Support biological and pharmaceutical developmental programs while ensuring regulatory compliance. • Collaborate with clinical research teams and provide input on site selection and study initiation. • Conduct site evaluations, monitoring, and audit preparations while communicating relevant findings. • Develop territory to broaden selection of research study sites and resolve study-related issues. • Maintain a home office if working remotely and manage work activities effectively.

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.