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Connect with over 2,000 popular apps and software to improve productivity and automate workflows
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Finding qualified clinical trial auditors with the right mix of GCP certification, regulatory expertise, and multi-site capability is challenging. This Clinical Trial Auditor Application Form template helps pharmaceutical companies, contract research organisations (CROs), clinical research sites, and quality assurance departments efficiently screen and recruit experienced audit professionals.
Clinical trial auditing demands meticulous attention to regulatory detail, deep knowledge of Good Clinical Practice (GCP) guidelines, and the ability to identify quality gaps before regulatory inspections occur. This application template captures all the critical qualifications you need—from ICH-GCP certification status and FDA/EMA inspection experience to CAPA development proficiency and therapeutic area expertise.
Whether you're hiring for sponsor quality assurance, CRO audit teams, or independent auditing consultancies, this form ensures you collect standardised, complete applications that make comparing candidates straightforward. Conditional logic reveals relevant follow-up questions based on certification levels and experience, so you only see the information that matters.
Regulatory-focused screening: Capture specific experience with FDA, EMA, MHRA, and other regulatory body inspections, along with audit findings management and remediation expertise.
GCP certification validation: Collect certification details, issuing bodies, and expiry dates, with file upload fields for certificates and training records—ensuring compliance from day one.
Quality systems expertise: Assess familiarity with ISO 9001, ISO 14155, 21 CFR Part 11, and ICH guidelines, plus hands-on experience developing and implementing Corrective and Preventive Actions (CAPA).
Multi-site and therapeutic area experience: Understand travel capability, willingness to conduct international audits, and depth of experience across oncology, cardiology, rare diseases, and other therapeutic areas.
Efficient candidate evaluation: All applications are collected in one place, with responses exportable to your ATS, HRIS, or project management system via Paperform's native integrations or Stepper workflows.
Once applications are submitted, use Stepper—Paperform's AI-native workflow builder—to automate your recruitment process. Route applications to hiring managers based on therapeutic area or location, send auto-acknowledgment emails with next steps, update your candidate tracking spreadsheet or ATS, and trigger background check or reference request workflows. Stepper keeps your hiring pipeline moving without manual data entry, so your quality and HR teams stay focused on evaluating the best candidates.
Paperform integrates with tools healthcare recruiters already rely on: push candidate data to HubSpot or Pipedrive CRMs, log submissions in Google Sheets or Airtable, notify your team via Slack, or connect to specialist ATS platforms using webhooks and Stepper. Every application is stored securely with SOC 2 Type II compliance, ensuring candidate data is handled to the highest standards.
This Clinical Trial Auditor Application Form is ideal for:
Easily adapt this template to match your organisation's specific requirements. Add questions about software proficiency (CTMS, eTMF, EDC systems), language capabilities for international audits, or preferred start dates. Adjust conditional logic to surface questions relevant to your therapeutic focus or regulatory market, and apply your brand colours, logo, and fonts to create a cohesive candidate experience.
Paperform is SOC 2 Type II and GDPR compliant, giving you confidence that sensitive candidate information—including certifications, employment history, and references—is protected. Data residency controls and role-based permissions ensure only authorised team members access applications, meeting the high standards expected in regulated healthcare environments.
Ready to hire your next clinical trial auditor? Use this template to collect complete, compliant applications and build a world-class audit team that keeps your clinical trials inspection-ready.