Clinical Trial Manager - Remote

Overview

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

In Short

• Leads the Clinical Study Team for assigned projects.
• Manage overall study timelines and oversight of vendor deliverables.
• Manage external vendors and contract research organizations.
• Prepare / Review / Approve study documents.
• Coordinate and contribute to the design of study materials.
• Assist with protocol development and study report completion.
• Manage monitoring activities at clinical study sites.
• Provide guidance to Clinical Research Associates.
• Track patient enrollment and assist in data management activities.
• Plan and participate in investigator meetings.

Requirements

• Bachelor’s degree in a scientific discipline or equivalent.
• At least 5 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.