Third Party Specialist

WEP Clinical Inc.; United Kingdom; Remote; GBP 45,000 - 70,000; Full time

Benefits offered by this job

Group Private Medical Insurance

Group General Life Assurance

Group Critical Illness and Group In- s

Group Income Protection

Salary sacrifice pension scheme

Enhanced maternity & paternity pay

Paid volunteering day

Job summary

WEP Clinical is seeking a Third-Party Specialist to coordinate and monitor external partners supporting GxP activities. You will ensure documentation, qualification, and ongoing oversight of suppliers and contractors, enabling compliant, safe delivery of clinical services across trials and related operations.

The ideal candidate will have a relevant degree, 2–5 years in a regulated quality role, and strong collaboration skills to work with Quality, Regulatory, Clinical, and Operations teams.

Qualifications

• Bachelor’s degree in pharmaceutical/life sciences or engineering.
• 2–5 years’ experience in a Quality role within a regulated (GxP) environment.
• Hands-on experience in vendor/supplier management.
• Strong knowledge of GMP, GDP and relevant national regulations.

Responsibilities

• Manage qualification and requalification of suppliers and vendors with documentation.
• Maintain and update Approved Supplier and Vendor Lists.
• Coordinate third-party risk assessments, questionnaires and due diligence.
• Monitor supplier performance via metrics and periodic reviews.
• Support CAPAs related to third-party findings.
• Plan and coordinate internal and external audits with vendors.
• Review audit records and follow up on findings.
• Contribute to inspection readiness and act as SME when required.
• Collaborate with Quality, Regulatory, Clinical, and Operations teams.
• Drive improvements in third-party management processes and metrics.

Skills

Proactive

Cross-functional collaborator

Adaptable

Critical thinker

Education

Bachelor’s degree in pharmaceutical sciences, life sciences, or engineering

Job description

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring ideas that make a real difference. Be part of a mission-driven organisation dedicated to advancing clinical research and transforming lives.

Role Objectives:

The Third-Party Specialist willbe responsible forthe day-to-day coordination, documentation, and monitoring ofthird parties (i.e. suppliers andthird-partycontractors/vendors)supporting the company’sGxPactivities. This includes qualification, ongoing performance monitoring, and compliance oversightofthird parties involved in pharmaceutical manufacturing, distribution, clinical operations,nursingand related support services. The role ensures thatall third partiesoperatein accordance withapplicable regulatory requirements and company standards, enabling the safe, effective, and compliant delivery ofWEP Clinicalservices(e.g.across Expanded Access Programs, Clinical Trial management and supply, and nursing operations).

The Ideal Candidate:

• Proactive and solutions-driven
• Critical thinker
• Cross-functional collaborator
• Adaptable

What You'll Do:

• Manage the qualification and requalification of suppliers and vendors, ensuring all required documentation is in place.
• Maintain and update Approved Supplier and Vendor Lists in line with company procedures.
• Coordinate third-party risk assessments, questionnaires, and due diligence checks.
• Monitor supplier performance through metrics and periodic reviews, escalating issues when needed.
• Support and track corrective and preventive actions (CAPAs) related to third-party findings.
• Help plan and coordinate internal and external audits, including liaising with vendors and auditors.
• Review and maintain audit records, ensuring timely follow-up on findings.
• Contribute to inspection readiness activities and act as a Subject Matter Expert when required.
• Work closely with Quality, Regulatory, Clinical, and Operations teams to ensure third-party compliance supports business needs.
• Drive improvements in third-party management processes and provide quality metrics to support business decisions.

What You'll Need:

• Bachelor’s degree (preferably in pharmaceutical sciences, life sciences, or engineering)
• 2–5 years’ experience in a Quality role within a regulated (GxP) environment
• Hands-on experience in vendor/supplier management
• Strong knowledge of GMP, GDP, and relevant national regulations
• Excellent organisational skills and attention to detail
• Effective written and verbal communication skills
• Ability to manage multiple priorities and meet deadlines under pressure
• Proactive, solutions-driven mindset with strong critical thinking skills
• Strong interpersonal skills and the ability to collaborate across teams
• High level of integrity and discretion when handling confidential information

What We Offer:

• Group Private Medical Insurance
• Group General Life Assurance
• Group Critical Illness and Group Income Protection
• Salary sacrifice pension scheme
• Enhanced maternity & paternity pay
• Paid volunteering day

What Sets Us Apart:

WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalised service of a specialised provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.

We're Committed to Our Team:

WEP has many initiatives to encourage wellness, growth, development, and team relationships. Check out our LinkedIn life page to learn more about our team events and all that we do to support our employees.

How We Work at WEP Clinical:

At WEP Clinical, we look for individualswho are conscientious, exercise sound judgement, 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 Include:

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

Data Privacy Notice:

WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.

Privacy Policy: https://www.wepclinical.com/privacy-policy/

Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/

Important Note:

For Your Safety, Please Note:

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.

WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.