Global Study Delivery Lead

Parexel; Uxbridge; On-site; GBP 90,000 - 120,000; Full time

Job summary

Parexel is seeking a senior Study Management professional to oversee global clinical trials from startup to data release. You will coordinate cross-functional teams, mentor SOMs, manage budgets and vendors, and ensure inspection readiness. Strong English communication and CRO oversight experience are essential.

The role requires leadership across study management, operational strategy, and collaboration with CSTLs and investigators to deliver high-quality trial data on time.

Qualifications

• Bachelor’s or higher in a life sciences field with significant trial management experience.
• Experience overseeing CROs, vendors, budgets, and timelines.
• Fluency in written and spoken English; strong communication skills required.

Responsibilities

• Lead and coordinate global clinical trial execution from sourcing to data release.
• Provide quality oversight of regional operations and study level plans with cross-functional teams.
• Mentor SOMs and ensure study startup, monitoring, and training plans are developed.
• Own drug supply management, vendor oversight, and cost variance reviews.
• Drive inspection readiness and interoperability with CROs and vendors.
• Interface with study management, data management, and investigator meetings to ensure timely delivery.

Skills

Study management

Vendor oversight

Budget management

Team leadership

GCP knowledge

English fluency

Education

Bachelor's degree in life sciences or related field

Master's degree in life sciences or MBA (preferred)

Scientific/technical degree preferred

Job description

Parexel is seeking a senior Study Management professional to oversee global clinical trials from startup to data release. You will coordinate cross-functional teams, mentor SOMs, manage budgets and vendors, and ensure inspection readiness. Strong English communication and CRO oversight experience are essential.

The role requires leadership across study management, operational strategy, and collaboration with CSTLs and investigators to deliver high-quality trial data on time.