Responsibilities:
Responsible for all things related to assigned aspects of clinical trial monitoring and site management.
Will have a significant impact on the continued growth of the organization.
Remote role with occasional travel to the Brisbane, California headquarters.
Compliance and Monitoring:
Ensure compliance with standard protocol and regulatory and ICH GCP obligations.
Complete on-site and remote monitoring activities in compliance with the Clinical Monitoring Plan.
Escalate observed deficiencies and issues as appropriate.
Requirements:
Minimum Bachelor’s degree in a life science-related field or equivalent.
3+ years’ experience in a clinical trials research environment required.
Strong interpersonal, collaborative, and time management abilities

Freenome

At Freenome, they are dedicated to changing the entire landscape of cancer.