Senior Clinical Quality Assurance Associate

Role Objectives

The Senior Clinical Quality Assurance Associate is responsible for the oversight, implementation, and continuous improvement of GCP quality systems supporting global clinical operations across all clinical activities, including decentralised clinical trials (DCTs) that involve nursing services and in-home patient care. This role provides quality leadership to operational teams by ensuring compliance with ICH GCP, applicable global regulatory requirements, Sponsor expectations, and internal Quality Management System (QMS) processes.

The Ideal Candidate

Attention to detail
Process-driven
Accountable
Collaborative

What You'll Do

• Serve as GCP quality systems SME across global clinical operations.
• Provide QA oversight to Clinical Operations, Nursing, Project Management, Medical Affairs, Pharmacovigilance, Regulatory Affairs, and other operational teams.
• Lead investigations for non-conformances, complaints, protocol deviations, quality events, and compliance issues.
• Independently manage complex CAPAs from investigation through effectiveness checks and closure.
• Lead risk assessments for new services, processes, vendors, systems, and operational changes.
• Review clinical and GCP documentation, including protocols, ICFs, eCRFs, Pharmacy Manuals, Monitoring Plans, and essential documents.
• Oversee decentralized clinical trial activities, including nursing, home healthcare, source documentation, IP handling, and related processes.
• Support QMS records and documentation, including deviations, CAPAs, complaints, change controls, risk assessments, SOPs, forms, templates, and guidance documents.
• Review change controls, support approvals, and lead post-implementation effectiveness reviews.
• Support vendor qualification, audits, requalification, Quality Technical Agreements, and ongoing vendor performance monitoring.
• Support audits and inspections by managing readiness, documentation, responses, corrective action plans, evidence, and commitment tracking.
• Review quality metrics, identify trends and risks, drive improvements, support validation/qualification activities, mentor QA staff, represent Quality on cross-functional projects, escalate significant risks, and promote a culture of quality and compliance.

What You'll Need

• Bachelor's Degree or higher (preference for pharmaceutical, life sciences, or engineering concentration)
• 3 to 5 years of experience in a quality-related role within a CRO, pharmaceutical, biotechnology, or healthcare organization
• Experience supporting global clinical trials and decentralized clinical trial activities
• Experience supporting Sponsor audits, regulatory inspections, internal audits, and/or supplier audits
• Practical experience with quality investigations, CAPAs, root cause analysis, quality risk assessments, and continuous improvement
• Practical understanding of GCP regulations and global regulatory expectations, including ICH E6(R3), FDA, EU Clinical Trial Regulation, MHRA, GDPR where applicable, and related requirements
• Strong understanding of Quality Management Systems, risk-based quality management principles, and computerized system validation or validation lifecycle principles
• Working knowledge of GDP, warehousing, logistics, and clinical trial supply processes is advantageous
• Strong analytical, organizational, communication, stakeholder management, mentoring, and influencing skills, with the ability to manage multiple priorities, handle confidential information professionally, and apply a proactive, solutions-focused mindset

What We Offer

• Medical, dental, and vision insurance
• FSA, HSA
• Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance
• Group short-term and long-term disability insurance
• Group Life Insurance
• 401K safe harbor plan and company match
• Paid vacation, holiday, sick and volunteer time
• Paid maternity & paternity leave

How We Work at WEP Clinical

We look for individuals who are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment.

Our Services

• Access Programs
• Clinical Trial Services
• Patient Site Solutions
• Clinical Trial Supply
• Market Access and Commercialization
• Data Privacy Notice

Privacy Policy

We will never communicate with you via Microsoft Teams or text message
We will never ask for your bank account information at any stage of recruitment

How to Apply

To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn’s Easy Apply option. Please ensure your resume is in English.