Senior Clinical Trials Program Manager

Tulane University; New Orleans (LA); On-site; USD 90,000 - 130,000; Full time

Job summary

Tulane University is seeking a Senior Clinical Project Manager to oversee all aspects of clinical trial conduct at the TRIAD Center, ensuring regulatory compliance, patient safety, data quality, and effective personnel management across multiple sites.

Under direction of senior leadership, the role requires advanced knowledge of protocol requirements, GCP, and IRB processes, with a track record of delivering studies on time and within budget.

Qualifications

• Bachelor’s degree required.
• At least three years of management experience.
• Cardiovascular or clinical research experience preferred.

Responsibilities

• Manage all aspects of clinical trial conduct across multiple studies and sites.
• Ensure regulatory compliance, patient safety, data quality and personnel management.
• Coordinate with Center Director and Associate Director to implement operational plans and timelines.
• Maintain relationships with IRB, investigators, sponsors, vendors, and stakeholders.

Skills

FDA/ICH GCP knowledge

Regulatory compliance

Leadership

Communication

Budget/Finances

Education

Bachelor's degree

Job description

Tulane University is seeking a Senior Clinical Project Manager to oversee all aspects of clinical trial conduct at the TRIAD Center, ensuring regulatory compliance, patient safety, data quality, and effective personnel management across multiple sites.

Under direction of senior leadership, the role requires advanced knowledge of protocol requirements, GCP, and IRB processes, with a track record of delivering studies on time and within budget.