Clinical Data QC Specialist - GxP & 21 CFR 11 Compliance
Clinical Data QC Specialist - GxP & 21 CFR 11 Compliance

Clinical Data QC Specialist - GxP & 21 CFR 11 Compliance

Full-Time 35000 - 45000 £ / year (est.) No home office possible
Moderna Therapeutics

At a Glance

  • Tasks: Ensure data quality and integrity in clinical laboratory settings.
  • Company: Join Moderna Therapeutics, a leader in innovative healthcare solutions.
  • Benefits: Enjoy generous paid time off and family building benefits.
  • Other info: Work in a dynamic environment with opportunities for growth.
  • Why this job: Make a difference in healthcare by ensuring high-quality analytical data.
  • Qualifications: 3+ years of lab experience and knowledge of GxP compliance.

The predicted salary is between 35000 - 45000 £ per year.

Moderna Therapeutics is seeking a detail-oriented professional with over 3 years of clinical laboratory experience for a role focused on analytical data quality in Oxford, England. The ideal candidate will have extensive knowledge of data integrity standards and quality control review in GxP regulated environments, expertise in lab-based techniques such as LC/MS and immunoassays, along with proficiency in Microsoft Office tools.

The position offers generous paid time off and family building benefits.

Clinical Data QC Specialist - GxP & 21 CFR 11 Compliance employer: Moderna Therapeutics

Moderna Therapeutics is an exceptional employer that prioritises employee well-being and professional growth, offering a supportive work culture in the vibrant city of Oxford. With generous paid time off and family building benefits, employees are encouraged to maintain a healthy work-life balance while engaging in meaningful work that contributes to innovative healthcare solutions.
Moderna Therapeutics

Contact Detail:

Moderna Therapeutics Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Data QC Specialist - GxP & 21 CFR 11 Compliance

✨Tip Number 1

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

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of GxP and 21 CFR 11 compliance. We recommend practising common interview questions related to data integrity standards and quality control review to show you’re the right fit.

✨Tip Number 3

Showcase your lab skills! If you’ve got experience with LC/MS and immunoassays, make sure to highlight that in conversations. We want to see you confidently discussing your technical expertise during interviews.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re here to help you every step of the way, so let’s get you that Clinical Data QC Specialist role!

We think you need these skills to ace Clinical Data QC Specialist - GxP & 21 CFR 11 Compliance

Analytical Data Quality
Data Integrity Standards
Quality Control Review
GxP Regulations
LC/MS Techniques
Immunoassays
Microsoft Office Proficiency
Clinical Laboratory Experience
Attention to Detail
Regulatory Compliance

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your clinical laboratory experience and any specific skills related to GxP and 21 CFR 11 compliance. We want to see how your background aligns with the role, so don’t be shy about showcasing your expertise in lab techniques like LC/MS and immunoassays.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about data quality and how your experience makes you the perfect fit for this role. We love seeing genuine enthusiasm, so let your personality come through!

Showcase Your Attention to Detail: As a Clinical Data QC Specialist, attention to detail is key. In your application, highlight examples where your meticulous nature has made a difference in your previous roles. We’re looking for candidates who understand the importance of data integrity standards.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, we love seeing applications come in through our own platform!

How to prepare for a job interview at Moderna Therapeutics

✨Know Your GxP and 21 CFR 11

Make sure you brush up on your knowledge of Good Practice (GxP) regulations and 21 CFR 11 compliance. Be ready to discuss how these standards apply to data integrity and quality control in clinical settings, as this will show your understanding of the role's requirements.

✨Showcase Your Lab Skills

Prepare to talk about your hands-on experience with lab techniques like LC/MS and immunoassays. Bring specific examples of how you've used these methods in past roles to ensure data quality, as this will demonstrate your practical expertise.

✨Be Proficient with Microsoft Office

Since proficiency in Microsoft Office tools is a must, be ready to discuss how you've used these applications in your previous work. Consider mentioning any specific projects where you utilised Excel for data analysis or PowerPoint for presentations.

✨Ask Insightful Questions

Prepare some thoughtful questions about Moderna Therapeutics' approach to data quality and compliance. This not only shows your interest in the company but also gives you a chance to assess if their values align with yours.

Clinical Data QC Specialist - GxP & 21 CFR 11 Compliance
Moderna Therapeutics

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