At a Glance
- Tasks: Lead strategic Quality oversight for global clinical trials, ensuring compliance and patient safety.
- Company: Join Novartis, a leader in innovative medicine with a commitment to quality.
- Benefits: Competitive salary, performance bonuses, flexible working, and comprehensive benefits package.
- Other info: Inclusive work environment with opportunities for personal and professional growth.
- Why this job: Make a real impact on patient outcomes while shaping the future of clinical development.
- Qualifications: Advanced degree in life sciences and significant experience in clinical research or quality assurance.
The predicted salary is between 78400 - 145600 £ per year.
Shaping the future of clinical development requires more than oversight—it demands leadership that can influence quality, drive decisions, and protect patient outcomes at scale. As Director, Development Unit CQA Program Lead, you will provide strategic Quality oversight across global clinical trials, ensuring compliance, data integrity, and patient safety remain at the forefront. Working in close partnership with Global Clinical Teams, you will guide critical risk-based decisions, strengthen governance, and embed a proactive quality mindset—ultimately enabling the successful delivery of innovative medicines to patients worldwide.
Key Responsibilities
- Provide strategic Quality leadership across assigned global clinical trials, ensuring compliance and patient safety throughout execution.
- Lead implementation of risk-based Quality strategies within Global Clinical Teams to support effective trial delivery.
- Oversee Quality risk management activities, including risk assessments, issue mitigation, and inspection readiness.
- Partner with cross-functional stakeholders to identify, manage, and resolve critical Quality risks and issues.
- Establish and lead governance for major Quality matters, ensuring timely escalation and resolution.
- Lead Quality aspects of regulatory inspections, audits, and follow-up activities, including corrective and preventive actions.
- Drive continuous improvement by embedding a strong Quality mindset and sharing lessons learned across programmes.
Essential Requirements
- Advanced degree in life sciences, medicine, pharmacy, or business administration.
- Significant experience in regulated clinical research, pharmacovigilance, or quality assurance within pharmaceutical development.
- Strong understanding of global clinical trial processes and regulatory requirements.
- Proven ability to lead and influence cross‑functional, global teams and stakeholders.
- Excellent communication and stakeholder management skills, including engagement with senior leadership and external authorities.
- Demonstrated ability to manage complexity, drive decision-making, and deliver continuous improvement initiatives.
Benefits & Rewards
At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. Expected Annual Base Salary Range for role: £78,400 to £145,600. The base salary offered is determined based on gender‑neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Long-term equity awards granted at group level may also be part of your package. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Director, Development Unit CQA Program Lead employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
StudySmarter Expert Advice🤫
We think this is how you could land Director, Development Unit CQA Program Lead
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We think you need these skills to ace Director, Development Unit CQA Program Lead
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Meeveem Limited!
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Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Meeveem Limited, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meeveem Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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