See all roles

Director, Global Clinical Operations Quality Management

Work from home Full-time role Hiring

When our values align, there's no limit to what we can achieve.   At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Strategic leadership of GCO Quality Management

  • Collaborate with GCO leadership to develop and implement the strategy and direction for the GCO QM team

  • Execute GCO QM mission and vision, including oversight of Global Support Centers

  • Propose, lead, and implement GCO QM initiatives aligned with GCO priorities

People leadership and development

  • Attract, recruit, retain, and develop qualified GCO QM staff

  • Ensure staff are appropriately trained, resourced, and deployed

  • Provide performance feedback, coaching, and succession planning

Quality issue management and oversight

  • Provide end-to-end oversight of quality issue management including triage, severity, categorization, RCA, and closure

  • Assign and prioritize QM resources based on risk and impact

  • Ensure timely and effective corrective and preventive actions

Quality risk identification, trending, and continuous improvement

  • Conduct trend analysis of GCO quality issues and audit findings

  • Identify systemic quality risks and emerging risk areas

  • Recommend and support process and system improvements

Audit and inspection readiness and support

  • Support audit and inspection preparation and execution

  • Ensure timely, high-quality responses and actions

  • Oversee implementation and effectiveness of audit actions

Ad hoc quality assessments and consultancy

  • Conduct ad hoc quality assessments

  • Recommend and oversee corrective actions

  • Provide quality consultancy to GCO leadership and teams

Oversight of site assessments

  • Oversee planning, conduct, and reporting of site assessments

  • Ensure appropriate follow-up actions are implemented

Global Support Center (GSC) oversight

  • Work closely with Global Support Centers, particularly APAC

  • Ensure quality delivery meets GCO standards

Compliance and professional standards

  • Exemplify compliance with Parexel standards, SOPs, and ICH GCP

  • Ensure accurate time recording and training completion

Additional responsibilities

  • Perform other quality-related responsibilities consistent with a Director-level role

Skills:

  • Excellent communication skills, including executive-level verbal and written communication, active listening, providing constructive feedback and facilitating group discussions.

  • Expert ability to think globally, strategically and analytically to problem-solve, make decisions keeping the patient and customer in focus. 

  • Excellent interpersonal skills, able to develop relationships and partnerships, build rapport, persuade and influence operational leaders, motivate others, manage performance and develop talent.

  • Effective change leader, able to understand and implement change while anticipating and managing resistance.

  • Expert manager with strong organizational and planning skills, competency in risk management with thoughtful action planning.

  • Personal awareness and emotionally intelligent, ability to self-motivate, innovate, delegate, and manage time as well as taking ownership and accountability for deliverables.

  • Ability to travel 10%-15%

Knowledge and Experience:

  • 15+ years’ experience in late phase clinical research

  • 7-10 years’ experience managing people

  • Expertise in ICH-GxPs

  • English proficiency (written and oral)

Education:

  • Bachelor’s Degree or other relevant experience required. Life science or other health-related discipline preferred.

  • Master’s Degree in a science, technology or industry-related discipline preferred.

Apply To This Job

You might like

Clinical Compliance Manager - UK or South Africa (Home-based) - FSP

Work from home Full-time role

Clinical Specialist Dental (m/w/*) - Region Mitteldeutschland (Kassel, Frankfurt, Würzburg, Leipzig)

Work from home Full-time role

Senior Data Scientist

Work from home Full-time role

Przedstawiciel ds. Kluczowych Klientów - województwo śląskie (m/k/x)*

Work from home Full-time role

Manager - Technical Accounting

Work from home Full-time role

Clinical Specialist Surgical Navigation and Robotics (Western Europe)

Work from home Full-time role

Sterilization Engineer II

Work from home Full-time role

Intern: Non-Tech

Work from home Full-time role

Territory Manager Spine

Work from home Full-time role

Sr. Engineer – Full Stack Development

Work from home Full-time role

Senior Data Engineer - Remote Opportunity at Tesla: Revolutionizing Sustainable Energy through Data-Driven Innovation

Work from home Full-time role

Communications Assistant, The Contrarian

Work from home Full-time role

Remote Jobs in Document Review (405) Oakland, CA

Work from home Full-time role

Immediate Hiring: Alliance Marketing Intern, Spring 2025

Work from home Full-time role

[Work From Home] Registered Nurse Telehealth

Work from home Full-time role

Experienced Part-Time Remote Data Entry Specialist – Join the Magic Behind the Scenes at blithequark

Work from home Full-time role

Full-Time Virtual Chat Support Associate – Remote Customer Experience & Technical Assistance Specialist

Work from home Full-time role

[Hiring] Auditor Clinical Validation DRG @Cotiviti

Work from home Full-time role

Hampden Front Desk Associate/ Youth Program Instructor – Amazon Store

Work from home Full-time role

Corporate Trainer, Work from Home

Work from home Full-time role