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Innovative Trials

Global patient recruitment, retention, and support.

Quality Assurance and Vendor Management Associate

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeLetchworth Garden City, UKHybrid

About the Job

Requirements

  • At least 2 years of quality assurance or vendor management experience within the pharmaceutical, biotechnology, or clinical research industry.
  • A solid working understanding of Good Clinical Practice and ISO 9001 standards, and familiarity with data privacy regulations such as GDPR and HIPAA.
  • High proficiency in Google Workspace and Microsoft Office, with the aptitude to learn specialised software and electronic systems.
  • Strong attention to detail and organisational skills.
  • Clear, confident written and verbal communication, and the ability to constructively challenge processes and maintain standards.
  • Resilience and composure under pressure, and the ability to balance shifting priorities in a fast-paced environment.
  • A proven track record of seeing projects and actions through to completion.

Responsibilities

  • Maintain and track CAPA, Change Control, and Quality Event logs; follow up with action owners to ensure timely closure and effectiveness assessments.
  • Organise investigation meetings for client complaints and internal non-conformances, draft detailed reports, and coordinate corrective and preventive actions.
  • Manage the end-to-end review lifecycle for SOPs and controlled documents, update the Controlled Document Matrix, and maintain Good Clinical Practice-compliant document repositories in Google Drive.
  • Assist with internal and external audit documentation, client RFI submissions, quality assurance archiving, and software purchasing and validation processes.
  • Assist in preparing Quality Review Meeting presentations, perform risk assessments, and provide quality guidance across teams on data protection, AI governance, and regulatory queries.
  • Review prospective vendor onboarding, liaise with department heads to identify procurement needs, and maintain the Approved Vendor List with timely re-qualifications and audit support.
  • Monitor vendor delivery, lead governance meetings with key operational vendors, negotiate vendor rebates, and manage a compliant catalogue of participant retention items.
  • Collaborate with stakeholders on the Environmental, Social, and Governance program; monitor and report Scope 1, 2, and 3 emissions; and track vendor ESG responsibilities and KPIs.

About the Company

Innovative Trials

Global patient recruitment, retention, and support.

Innovative Trials focuses on helping clinical trials recruit and keep participants. It works with sponsors, CROs, and sites by providing engaging recruitment and retention materials, hands-on 1:1 site coaching, and a global Patient Support Center with in-country support across 70+ countries and in more than 120 languages. The team acts as an extension of the study group, emphasizing practical collaboration rather than acting as a distant vendor. Privately owned, it stays flexible and focused on what benefits clients and patients, not just board reports. Its goal is to keep the human side of trials alive by reassuring patients, supporting sites, and helping study teams meet recruitment targets efficiently.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
England, United Kingdom
Founded
2010

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