Clinical Trial Manager

Direct experience of running early-stage clinical trials within an industry environment.

Strong working knowledge of FDA Regulations, ICH Guidelines and GCPs governing the conduct of clinical trials.

Experience in selection of CROs/ vendors and management of external resources.

A demonstrable record of strong vendor management and teamwork.

Direct experience of managing clinical CROs.

Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.

This is a unique opportunity for an experienced Clinical Operations Professional who has technical expertise in managing Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operations, Good Clinical Practice (GCP) and U.S.

Food and Drug Administration (FDA) regulatory requirements.

As the Clinical Trial Manager of Clinical Operations, initially reporting to the Director, Clinical Operations, you will be responsible for Contract Research Organization (CRO) oversight and execution of Revolution Medicines clinical studies.

Clinical operations functional activities related to the execution of assigned clinical trials based upon department and corporate goals and objectives.

Management of clinical studies and vendors to ensure studies are completed on time, within budget and in compliance with Standard Operating Procedures (SOPs), FDA regulations and International Council for Harmonization (ICH)/ GCP guidelines.

Identify, engage, and manage the activities of clinical CROs and other clinical study providers (e.g., core labs, Electronic Data Capture (EDC) provider, and independent contractors) to execute clinical trials.