Global CAT Operations Lead for Clinical Trials

Worldwide Clinical Trials; Poland; Remote; PLN 180,000 - 300,000; Full time

Job summary

Worldwide Clinical Trials is seeking a senior lider in CAT Operations to drive operational excellence across global clinical trials. You will oversee study deliverables from launch to close-out, coordinate resourcing, manage budgets and vendor relationships, and lead cross‑functional initiatives with Contracts, PM and QA teams.

The role requires 7+ years in clinical trials, including 4+ years in global studies, and strong leadership and CFR/GCP knowledge.

Qualifications

• Bachelor’s degree; Master’s degree preferred in life sciences, MBA and/or PMP.
• 7+ years of clinical trial experience with 4+ years in global trials.
• Experience leading teams or managing projects in a CRO/clinical trials setting.
• Experience in psychiatry/CNS is a plus.
• Strong leadership, planning and interpersonal abilities.
• Knowledge of CFRs, GCPs and ICH guidelines.

Responsibilities

• Identify operational needs for upcoming projects and allocate resources.
• Provide operational oversight for CAT study projects from launch to close‑out.
• Coordinate resourcing, training and skills development for CAT Operations staff.
• Lead process improvement and participate in QMD reviews and document development.
• Collaborate with Operations, Project Management and Contracts on budgets and scope changes.

Skills

Organizational skills

Management skills

Planning skills

Time management

Interpersonal skills

Statistics knowledge

Finance practices

Vendor management

Education

Bachelor's degree

Master's degree in life sciences

MBA

PMP certification

Job description

Worldwide Clinical Trials is seeking a senior lider in CAT Operations to drive operational excellence across global clinical trials. You will oversee study deliverables from launch to close-out, coordinate resourcing, manage budgets and vendor relationships, and lead cross‑functional initiatives with Contracts, PM and QA teams.

The role requires 7+ years in clinical trials, including 4+ years in global studies, and strong leadership and CFR/GCP knowledge.