Global Study Lead: Trial Management & Vendor Oversight

Parexel; Montgomery (AL); On-site; USD 110,000 - 170,000; Full time

Job summary

Parexel is seeking a Global Study Manager II to provide operational leadership across the study lifecycle. You will oversee study management, site management, CRO/vendor deliverables, and ensure timely, high-quality data delivery for global trials.

The role requires extensive experience in clinical study management, vendor oversight, and budget control, with strong communication and leadership skills to coordinate cross-functional teams and investigators. Travel may be required.

Qualifications

• Bachelor’s degree in life sciences; 7+ years relevant operational clinical trial experience or Master’s degree with 6+ years.
• Experience in clinical research, study management, and oversight of CROs and vendors.
• Fluency in written and spoken English; ability to travel as required.

Responsibilities

• Lead and coordinate global execution of clinical trials from sourcing to outsourced studies and vendor deliverables.
• Provide quality oversight of regional operations and CRO tasks for study execution.
• Set recruitment targets and milestones; oversee study start up, monitoring, and other study plans.

Skills

Clinical study management

Vendor oversight

Budget management

Project leadership

GCP knowledge

Fluent English

Education

Bachelor’s degree in life sciences

Master’s degree in a relevant field

Tools

CTMS

IMS/IRT systems

Job description

Parexel is seeking a Global Study Manager II to provide operational leadership across the study lifecycle. You will oversee study management, site management, CRO/vendor deliverables, and ensure timely, high-quality data delivery for global trials.

The role requires extensive experience in clinical study management, vendor oversight, and budget control, with strong communication and leadership skills to coordinate cross-functional teams and investigators. Travel may be required.