Job Description
GCP Quality Manager - Leading Clinical Trials Innovator
Location: London, UK
Contract Type: Permanent
Salary: 55000
- Join a dynamic, mission-driven team dedicated to transforming clinical trial infrastructure
- Contribute to the development and implementation of robust GCP quality assurance processes
- Enjoy a supportive culture with unlimited holidays, flexible working, and personal development opportunities
- Benefit from competitive salary, generous stock options, and UK visa sponsorship for eligible candidates
Our client, a leading clinical trials innovator, is seeking a proactive and passionate GCP Quality Manager to join their growing team in London. This is an exciting opportunity to play a key role in ensuring the company's clinical trials consistently meet the highest regulatory standards.
Position Overview
As the GCP Quality Manager, you will be instrumental in developing and implementing quality assurance processes and procedures that are fully compliant with GCP and relevant regulations. Your expertise will help ensure that the company's clinical trials are conducted to the highest standards, ultimately contributing to the advancement of innovative healthcare treatments.
Responsibilities
- Support the development and implementation of GCP-compliant quality assurance processes and procedures
- Stay updated on national and international legislation, guidelines, and customer practices, providing consolidated information to the Quality & Clinical Operation Team
- Ensure the company's delivered studies consistently meet all regulatory requirements
- Maintain accurate and up-to-date documentation related to GCP and quality management processes
- Review study documents within the Clinical Operations Team to ensure compliance with current clinical trial regulations
- Support internal and external audits, preparing staff and trial materials for inspections by Sponsors and regulatory bodies
- Identify and assess risks associated with GCP, implementing risk mitigation strategies in collaboration with cross-functional teams
Requirements
- 3-5 years experience in GCP Quality roles
- Expertise in ICH GCP and multiple regional areas (MHRA and FDA experience beneficial)
- Demonstrated experience in Sponsor and regulatory GCP audits
- High agency and a proactive attitude
- Deep passion and curiosity for transforming healthcare operations and advancing new health treatments
- Desire to contribute to the dynamic environment of a high-growth, mission-driven, venture-capital-funded startup
Company Overview
Our client is a young and ambitious company founded in March 2021, dedicated to revolutionising the clinical trial landscape. With a mission to help innovative companies run faster, more reliable, and patient-friendly clinical trials, they have already made significant strides, successfully facilitating over 80 clinical trials involving thousands of patients. Their commitment to excellence has earned them an impressive customer NPS of 100 and recently secured $18 million in Series A funding to fuel their growth.
Benefits
- Competitive salary and generous stock options
- Unlimited holidays, with encouragement to take at least 28 days off each year
- Flexible office arrangement, with a 3-4 day per week in-office commitment initially
- Regular team events and opportunities for personal development through courses
- Provision of a new laptop and financial support for setting up a home office
- UK visa sponsorship for eligible candidates not already authorised to work in the UK
You'll be part of a dynamic, mission-driven team that values proactivity, personal development, and a deep passion for transforming healthcare. The company fosters a supportive and engaging work environment, offering regular team events and opportunities for growth.