Senior Clinical Trial Manager - Remote

Overview

The Senior Clinical Trial Manager is responsible for the execution and management of assigned clinical studies while ensuring Good Clinical Practices (GCP) Compliance, high study quality, and timely completion.

In Short

• Leads the Clinical Study Team for assigned projects.
• Manage external vendors and contract research organizations.
• Prepare/Review/Approve study documents.
• Coordinate and design study materials.
• Assist with protocol development and study report completion.
• Manage monitoring activities at clinical study sites.
• Provide guidance to Clinical Research Associates (CRAs).
• Track patient enrollment and manage closeout activities.
• Coordinate study supplies and manage contracts.
• Participate in investigator meetings.

Requirements

• Bachelor’s degree in a scientific discipline required.
• At least eight years of biopharma industry experience.
• Vendor management experience in clinical operations.
• Strong verbal and written communication skills.
• Ability to build and maintain strong working relationships.
• Must be able and willing to travel periodically.
• Experience with Microsoft Office Suite required.

Benefits

• Patient Days to hear from individuals living with conditions.
• A culture inspired by values: put patients first, think independently.
• Access to learning and development resources.
• Robust and market-competitive compensation & benefits package.
• Flexible PTO.
• Rapid career advancement for strong performers.
• Commitment to Diversity, Equity & Inclusion.