Clinical Study Manager

Actalent - Basking Ridge, NJ

Full-time - Mid Level

Remote - Basking Ridge, NJ

10,001+ employees

Administrative and Support Services

About the position

As a Clinical Study Manager at Actalent, you will be responsible for the planning and execution of clinical studies, particularly in the oncology field. This role involves developing integrated study plans, overseeing site selection, ensuring compliance with operational protocols, and managing study budgets. You will coordinate with internal stakeholders and external CROs to ensure timely delivery of study items while supporting knowledge management and departmental training efforts.

Responsibilities

• Develop a cross-functional, integrated study plan for clinical studies.
• Oversee site selection and qualification processes.
• Ensure operational delivery aspects of the protocol are met.
• Act as a project manager for the clinical study team.
• Coordinate with internal stakeholders and oversee CRO activities.
• Ensure compliance with quality measures and manage study budgets.
• Provide oversight for CRO-generated documents.
• Support knowledge management and departmental training efforts.

Requirements

• Experience in global clinical trial management.
• Background in oncology.
• Phase III clinical trial experience.
• Strong vendor management skills.

Benefits

• Fully remote position
• Contract-to-Hire opportunity with a duration of 9 months