Find your dream job faster with JobLogr
AI-powered job search, resume help, and more.
Try for Free
AR

argenx

via Workday

All our jobs are verified from trusted employers and sources. We connect to legitimate platforms only.

Clinical Quality Lead

Anywhere
Full-time
Posted 12/22/2025
Direct Apply
Key Skills:
GCP compliance
Clinical trial quality assurance
Audit management
Regulatory inspection readiness
Vendor qualification

Compensation

Salary Range

$152K - 228K a year

Responsibilities

Oversee clinical trial quality assurance activities, including audits, vendor management, and regulatory inspections, ensuring compliance with GCP and regulatory standards.

Requirements

Minimum 7 years of clinical trial experience, with at least 5 years in quality assurance, and FDA/EMA inspection experience.

Full Description

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases. We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients. 1.PURPOSE OF THE FUNCTION Drive towards real time quality oversight and consistent high-quality standards of the global clinical trials, both pre and post marketing Provide GCP oversight for an argenx asset (applicable based on assignment), act as GCP SME, support audit and inspection planning and execution, and manage clinical quality event investigations and remediation. Oversee relationship and performance of clinical partners vendors/suppliers. GCP Quality Point of Contact (POC) for assigned Business Partners. 2.REPORTING LINE Head of R&D Quality 3.ROLES AND RESPONSIBILITIES Serve as the primary Quality point of contact for assigned clinical trials Guide the Clinical Trial Team (CTT) to ensure clinical trials are conducted in compliance with GCPs, regulatory requirements, and argenx processes Lead the GCP quality oversight for assigned clinical trials, collaborating closely with CTT(s) to uphold high-quality standards Manage the clinical trial audit programs, including leading the audit site selection process for study-specific audit plans in collaboration with CTT(s), and ensuring timely audit conduct, reporting, review, and closeout in accordance with argenx processes Oversee or lead the qualification/re-qualification of vendors as necessary Participate in and lead audits to maintain compliance and quality Work with CTT(s) to produce GCP quality system metrics for real-time quality monitoring and reporting (e.g., audits, deviations, CAPAs), and conduct trend analysis for management reporting Drive the investigation of trial quality events and define necessary corrective and preventive measures Lead clinical trial inspection readiness activities to ensure preparedness Provide QA input during the creation/revision of argenx clinical procedural documents for GCP compliance When assigned as “QA Approver” in ARGO or PhoeniQS, act as QA approver for GCP area. Act as a delegate for R&D Quality head for the Document Review Committee (DRC) Participate/lead in regulatory inspections Oversee the relationship and performance of clinical partners/vendors to maintain quality standards Support and own key GCP Quality processes per assignment and offer solutions/improvement from a continuous improvement mindset Provide metrics and trends for continuous improvement, sharing lessons learned and best practices among other CTT(s). Ability to mentor junior quality leads upon delegation by the R&D quality head. 4.SKILLS AND COMPETENCIES In‐depth knowledge of Clinical Trial related US and EU regulations and ICH GCP Guidelines Preferred: Knowledge of global pharmacovigilance regulations Ability to create a comprehensive study quality oversight plan and audit program and lead the execution Ability to influence without direct leadership: motivate and educate the clinical study team on clinical quality aspects Proven capability to establish and maintain effective relationships with both internal and external stakeholders Demonstrated ability to thrive in a dynamic environment within a rapidly growing biotech company, effectively managing challenging timelines. 5.EDUCATION, EXPERIENCE AND QUALIFICATIONS MS Degree Minimum 7 years clinical trial experience Minimum 5 years quality assurance experience FDA, EMA, MHRA, PDMA Inspection experience LI-Onsite ‎ For applicants in the United States: The annual base salary hiring range for this position is $ 152.000,00 - $ 228.000,00 USD. This range reflects our good faith estimate at the time of posting. Individual compensation is determined using objective, inclusive, and job-related criteria such as relevant experience, skills, demonstrated competencies and internal equity. This means actual pay may differ from the posted range when justified by these factors. Because market conditions evolve, pay ranges are reviewed regularly and may be adjusted to remain aligned with external benchmarks. This job is eligible to participate in our short-term and long-term incentive programs, subject to the terms and conditions of those plans and applicable policies. It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines. At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer. Before you submit your application, CV or any other personal details to us, please review our argenx Privacy Notice for Job Applicants to learn more about how argenx B.V. and its affiliates (“argenx”) will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at privacy@argenx.com. If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@argenx.com. Only inquiries related to an accommodation request will receive a response. argenx is a global immunology company dedicated to improving the lives of people suffering from severe autoimmune diseases. Through our rich pipeline of first-in-class therapies, led by VYVGART®, we are accelerating progress toward our bold 2030 vision: to reach 50,000 patients and transform the landscape of autoimmune treatment. Our innovation mission combines with meaningful work and endless opportunities for growth to create once-in-a-career experiences. argonauts work in locations around the globe including Belgium, Boston, Japan and Amsterdam. There's more to discover at argenx, where our passion inspires bold possibility. argenx honors the terms of our written agreements with the recruiting and staffing agencies that we retain and contract with to assist us with talent searches and other recruiting needs. Accordingly, all resumes and referrals that recruiting and staffing agencies proactively share with argenx that (i) were not solicited or requested by argenx’s internal Talent Acquisition team and (ii) were sent in the absence of a valid, written agreement between argenx and the firm, recruiter, or agency, may be pursued by argenx and are ineligible for payment of referral or other fees. We encourage you to be cautious of recruiting scams and fictious communications that pretend to be from argenx employees. These scams are designed by fraudsters to get personal information (e.g., social security numbers, bank account information, dates of birth), money or payments from job seekers as part of a “recruiting” process. argenx does not request financial information or money from job seekers. Legitimate emails from argenx employees end in “@argenx.com.” Fraudsters disguise themselves by using similar email addresses (e.g., @argenxhr.com, @argenxcareer.com, etc.) or public domains (@gmail.com, @yahoo.com, etc.). They may use photographs and names of real argenx employees for their fake interviews. argenx does not recruit or post positions on RingCentral, Facebook, or Craig’s List. Our formal recruitment process includes interviews with members of argenx’s talent acquisition team and other interviewers that occur in person at our offices, or via Zoom or Teams video calls. Interview processes that involve a formal offer from argenx will include written employment documentation on official argenx letterhead. argenx takes prompt appropriate and responsive action to fraudulent recruiting efforts when we become aware of them. If you believe you have been victimized by an employment application or a fraudulent recruiting scam, you can contact your local law enforcement authority for guidance or the FBI’s Internet Crimes Complaint Center at www.IC3.gov to file a complaint.

This job posting was last updated on 12/23/2025

Ready to have AI work for you in your job search?

Sign-up for free and start using JobLogr today!

Get Started »
JobLogr badgeTinyLaunch BadgeJobLogr - AI Job Search Tools to Land Your Next Job Faster than Ever | Product Hunt