About this role

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.

Key Accountabilities:

QMSO Support processes

  • Support the execution of Parexel Quality's strategy and Parexel's QMS
  • As assigned, support execution of the strategic and tactical goals of QMSO for the key QMS elements, including, but not limited to: QMS infrastructure, Quality Issue Management, Management Review, Change Management, Process Optimization, Controlled Documents, Knowledge Management, and Risk Management.
  • Work to continuously improve Parexel’s QMS.
  • Maintain a familiarity with Parexel QMS-related systems and related
  • Provide coaching, mentoring and constructive feedback to QMSO staff as required.
  • Manage projects and initiatives as assigned, including participants, reporting and escalations as needed. Ensure that project / initiative resources are adequate. If they are not, escalate and either obtain the necessary resources or reprioritize work according to available resources.
  • Support management of the QMSO budget.

Parexel Quality Department Support

  • Support Corporate Quality in the attendance, preparation for and follow up of internal/external audits and inspections as required.
  • Work with Corporate Quality to develop and/or update quality/process documents, tools, and templates. Consider process for effectiveness measurement.
  • Provide technical knowledge and oversight (including Quality eQMS applications business leadership) and serve as an escalation point where appropriate.
  • Maintain a positive, results oriented work environment, building partnerships within the group and across the organization at large, modeling teamwork
  • Remain informed about developments in relevant regulations and guidelines.
  • Support Operations staff in the use of automated quality systems; summarize automated quality system reports and provide metrics as appropriate.
  • Work with the relevant training functions including Learning & Development. Assist with the development or enhancement of training materials as assigned.

Global Organization Support

  • Present QMS to clients, auditors and regulatory inspectors
  • Lead cross functional improvements projects as required

Skills:

  • Excellent interpersonal, verbal and written communication skills
  • Customer focused approach to work
  • A flexible attitude with respect to work assignments and new learning
  • Ability to manage and prioritize tasks efficiently and accurately
  • Willingness to work in a matrix environment and to value the importance of teamwork
  • Understanding of audit/inspection process
  • Ability to lead projects and teams
  • Strong ability to analyze and interpret data
  • Attention to detail and advanced organizational skills
  • Ability to work independently and take ownership of and responsibility for work assigned
  • IT literate – Experience with Microsoft based applications and a general knowledge of PC functions
  • Culturally aware and ability to think and work globally
  • English proficiency (written and oral English)

Knowledge and Experience:

  • 5 to 8 years work experience
  • Substantial experience in Clinical Research field (pharmaceutical industry or CRO) or other pertinent experience in the areas of QMS support required
  • Knowledge of GxP compliance as required
  • Relevant experience in Quality Management
  • Clinical Lead, Clinical Operations Lead, Lead CRAs (or equivalent roles) with extensive experience in Quality Events (Quality Issues or Audits/ Inspections Findings) would be considered relevant.
  • Technology / Business Operations experience, as appropriate, preferred
  • Leadership and/or project management experience preferred
  • Training experience required
  • Substantial experience working in a global environment

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 disciple preferred.

Frequently Asked Questions

Is the salary disclosed for the Quality Management System Oversight Lead position at parexel?
The salary for this Quality Management System Oversight Lead role at parexel is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Quality Management System Oversight Lead position at parexel located?
This Quality Management System Oversight Lead role at parexel is based in China-Beijing, China-Chengdu, China-Guangzhou, China-Shanghai Shinmay, China-Shenyang, Philippines-Manila, Thailand-Bangkok. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Quality Management System Oversight Lead role at parexel full-time or part-time?
This is listed as a Full time position. It is posted as a Quality Management System Oversight Lead role in the 1756 Parexel Shanghai Co. Ltd. department at parexel.
Which team or department does the Quality Management System Oversight Lead at parexel belong to?
This Quality Management System Oversight Lead position is part of the 1756 Parexel Shanghai Co. Ltd. department at parexel. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Quality Management System Oversight Lead position at parexel?
Click the "Apply Now" button on this page. You will be redirected to parexel's official application portal hosted on workday where you can submit your application directly.
When was the Quality Management System Oversight Lead job at parexel posted?
This Quality Management System Oversight Lead position at parexel was posted on Sep 8, 2026. Apply as soon as possible — early applications are often reviewed first.
Quality Management System Oversight Lead
parexel
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