Clinical Trials QA Leader – Associate Director in London
Clinical Trials QA Leader – Associate Director

Clinical Trials QA Leader – Associate Director in London

London Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead quality assurance for clinical trials and manage audits to ensure high standards.
  • Company: Major global pharmaceutical company with a strong reputation in the UK.
  • Benefits: Competitive salary, career advancement opportunities, and a dynamic work environment.
  • Why this job: Make a significant impact on clinical trials and enhance patient safety.
  • Qualifications: Experience in quality assurance and strong stakeholder management skills.
  • Other info: Join a team that values innovation and excellence in healthcare.

The predicted salary is between 43200 - 72000 £ per year.

A major global pharmaceutical company in the UK is seeking an Associate Director of Quality Assurance to oversee GCP activities and lead audits for clinical trials. The successful candidate will ensure high-quality execution of trials and manage cross-functional relationships while representing quality assurance at internal meetings. This role has significant impact and visibility, requiring adept management of both internal and external stakeholder relationships.

Interested candidates should send their CV to the provided email address.

Clinical Trials QA Leader – Associate Director in London employer: Cpl Life Sciences

As a leading global pharmaceutical company based in the UK, we pride ourselves on fostering a dynamic work culture that prioritises employee growth and development. Our commitment to quality assurance in clinical trials not only ensures impactful contributions to healthcare but also offers our employees unique opportunities for professional advancement and collaboration with cross-functional teams. Join us to be part of a mission-driven organisation that values innovation, integrity, and excellence.
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Contact Detail:

Cpl Life Sciences Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trials QA Leader – Associate Director in London

Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at events. We can’t stress enough how valuable personal connections can be in landing that dream role.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of GCP and quality assurance processes. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.

Tip Number 3

Showcase your leadership skills! During interviews, share specific examples of how you’ve successfully managed cross-functional teams or resolved conflicts. We want to see how you can bring that experience to the table.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate candidates who are ready to make an impact in clinical trials.

We think you need these skills to ace Clinical Trials QA Leader – Associate Director in London

Quality Assurance
Good Clinical Practice (GCP)
Audit Management
Cross-Functional Collaboration
Stakeholder Management
Communication Skills
Project Management
Attention to Detail
Problem-Solving Skills
Regulatory Compliance
Risk Management
Leadership Skills
Analytical Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of Clinical Trials QA Leader. Highlight your experience in GCP activities and any relevant audits you've led. We want to see how your skills align with what we're looking for!

Showcase Your Leadership Skills: As an Associate Director, you'll need to manage relationships across various teams. Use your application to demonstrate your leadership experience and how you've successfully navigated cross-functional collaborations in the past.

Be Clear and Concise: When writing your application, keep it clear and to the point. We appreciate straightforward communication, so avoid jargon and make sure your key achievements stand out. This will help us see your potential quickly!

Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications better and ensures you don’t miss any important updates from us during the hiring process!

How to prepare for a job interview at Cpl Life Sciences

Know Your GCP Inside Out

Make sure you brush up on Good Clinical Practice (GCP) guidelines before the interview. Be prepared to discuss how you've applied these principles in your previous roles, as this will show your expertise and commitment to quality assurance.

Showcase Your Audit Experience

Be ready to share specific examples of audits you've led or participated in. Highlight any challenges you faced and how you overcame them, as this demonstrates your problem-solving skills and ability to maintain high standards.

Understand Stakeholder Management

Since this role involves managing cross-functional relationships, think about how you've successfully collaborated with different teams in the past. Prepare to discuss strategies you've used to build rapport and ensure effective communication.

Prepare Questions for Them

Interviews are a two-way street! Prepare insightful questions about their current clinical trials and quality assurance processes. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Clinical Trials QA Leader – Associate Director in London
Cpl Life Sciences
Location: London

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