Pharmacovigilance Safety Manager

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS is seeking an experienced Pharmacovigilance Safety Manager to lead our Safety Team and oversee the Safety Management process for clinical trials. In this role, you will manage PV services, establish and maintain safety reporting processes, provide global safety guidance, and serve as the primary safety contact for sponsors, clinical teams, and subcontractors. You will also provide day-to-day leadership and support to a small Safety Team.This role may be filled in the US, Austria, Czech Republic or the Netherlands.QPS' StorySince its inception, QPS has been assisting pharmaceutical, biotechnology, and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical, and Phase II – IV Clinical Research services.To meet the needs of our clients, we strive to employ talented, caring, and committed individuals who work collaboratively toward our mission of improving human health and quality of life.Our team members enjoy challenging and rewarding work in a culture that values diversity, innovation, accountability, teamwork, and a friendly atmosphere where performance is recognized and rewarded. We offer unique company benefits, training, and opportunities for advancement. Most importantly, we value our team members both as employees and as individuals.If this sounds like your ideal work environment, we would love to speak with you. Apply today and visit to learn more about QPS Holdings, LLC. The JobOversee the PV Safety Management process for clinical trials, ensuring high-quality and compliant delivery of safety activitiesLead and support the Safety Team, providing day-to-day direction, guidance, and oversight of assigned workServe as the primary safety contact for sponsors, clinical project managers, the QPS Safety Team, and other involved partiesProvide guidance on global safety reporting requirements and ensure compliance with applicable regulations and guidelines, including GCP and EudraVigilance requirementsDevelop and maintain Clinical Safety Management Plans, safety databases, procedures, and related documentationLead clinical safety meetings and facilitate effective communication among sponsors, project teams, subcontractors, and other stakeholdersCollaborate with Finance and project teams on project setup, budgeting, and invoicing for PV servicesWork LocationThis job will be 100% home-office based. RequirementsStrong knowledge of international clinical safety reporting regulations and guidelines, including GCP and EudraVigilance, with the ability to serve as a go-to resource for global safety guidanceWorking knowledge of safety reporting requirements within clinical studiesProven experience in clinical trials, a CRO environment, or a related fieldExperience leading, supervising, or providing day-to-day direction to PV/safety team membersExcellent organizational and communication skills, including business-level EnglishStrong analytical thinking, with the ability to research, evaluate, and apply complex information effectivelyStrong attention to standards, quality, and impact, with demonstrated thoroughness and accuracyUniversity degree in a relevant discipline or equivalent combination of education and experienceWhy You Should ApplyOpportunities to learn and grow. Work alongside experienced professionals who will support your continued development and career goals.Structured Career Ladders that provide opportunities for growth based on your skills and aspirations.Performance-based rewards, including bonuses and merit increases linked to individual, team, and company performance.Solid benefits package, including Company-matched 401(k), Company-sponsored Group Life/AD&D, and Short- and Long-term Disability Insurance.Employee-focused internal committees designed around the needs, interests, and enjoyment of QPS employees.Join QPS and play an important role in ensuring safety, compliance, and quality across our clinical trials while helping lead and develop our growing Safety Team.For US candidates - QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with US/federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans. #LI-DNI