At a Glance
- Tasks: Connect with us for future opportunities in clinical quality assurance.
- Company: Join a global CRO dedicated to patient safety and well-being.
- Benefits: Competitive compensation, comprehensive benefits, and growth opportunities.
- Other info: Engage in genuine career conversations and be first in line for new roles.
- Why this job: Be part of a team that values trust, quality, flexibility, and passion.
- Qualifications: 5+ years in pharma, strong knowledge of ICH-GCP and drug development.
The predicted salary is between 59400 - 72600 £ per year.
Join Our Talent CommunityWe're not advertising a specific role today - we're proactively connecting with experienced professionals for upcoming opportunities. By joining our talent community, you'll be among the first considered when the right role opens. Who We're Looking to Connect WithProvides advice on clinical quality, ICH-GCP guidelines, and local regulatory requirements to study teamsSupports audits and inspections and acts as the main contact for auditorsDrives quality control activities and monitors compliance within clinical studiesIdentifies quality risks and ensures corrective and preventive actions are implementedDevelops, maintains, and implements local procedural documents and quality frameworksTypical QualificationsBachelor's degree in life sciences or a related disciplineAt least 5 years of experience in the pharmaceutical industry (Development Operations or Quality Assurance preferred)Strong knowledge of ICH-GCP and local clinical trial regulationsGood understanding of drug development processes and GxP requirementsExcellent communication, organisational, and problem-solving skillsWhat You Can Expect From UsA review of your profile by our Talent Acquisition teamDirect outreach when a relevant opportunity opens that matches your experienceA genuine career conversation, not a transactional oneWhen Will You Hear From Us? Because this is a proactive talent pool rather than a live vacancy, our response timelines work a little differently. A member of our Talent Acquisition team will then be in touch directly when a suitable opportunity arises, this could be in a few weeks, a few months, or longer depending on business needs. What We OfferWe provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. As a global CRO with the ultimate goal of ensuring patients' safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. Our core values of Trust, Quality, Flexibility and Passion are what make TFS HealthScience the successful company it is today.
Senior Clinical Quality Assurance Manager in London employer: Trial Form Support
TFS HealthScience is an exceptional employer, offering a dynamic work environment where innovation and collaboration thrive. As a Senior Clinical Research Associate, you will benefit from a competitive compensation package and comprehensive benefits, while also having the opportunity for personal and professional growth in a rewarding setting. With a strong emphasis on core values such as Trust, Quality, and Sustainability, TFS fosters a culture of mutual respect and engagement, making it a fulfilling place to advance your career in clinical research.
