Clinical Scientist - Oncology - Remote

Overview

The Clinical Scientist will leverage their scientific and medical expertise in oncology to lead and execute clinical development activities for one or more assigned studies in molecular residual disease monitoring or early cancer detection.

In Short

• Develop study concepts, including overall study design and objectives.
• Contribute to authoring of the study protocol and provide critical feedback.
• Provide protocol trainings to internal and CRO teams.
• Work with Clinical Operations to design study-specific case report forms.
• Ensure study manuals are aligned with the study protocol.
• Engage with key investigators on study design and methodology.
• Serve as clinical science representative in meetings.
• Contribute to real-time clinical data reviews.
• Support advisory boards and steering committee meetings.
• Deliver presentations at scientific meetings and represent the company at trade shows.

Requirements

• Ph.D./RN/MS required.
• 5-8 years experience as a Clinical Scientist preferred.
• Experience with project management and clinical research.
• Periodic travel (~15-20% including overnight travel).

Benefits

• Comprehensive medical, dental, vision, life and disability plans.
• Free testing for employees and their immediate families.
• 401k benefits and commuter benefits.
• Generous employee referral program.