Strategic Clinical Research Compliance Lead
Strategic Clinical Research Compliance Lead

Strategic Clinical Research Compliance Lead

Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead compliance in clinical research and ensure data integrity with ICH GCP guidelines.
  • Company: Top clinical research organisation based in London, focused on innovation.
  • Benefits: Competitive salary, comprehensive benefits, and opportunities for professional growth.
  • Why this job: Make a real difference in clinical research while ensuring high standards of compliance.
  • Qualifications: BSc or higher in Life Sciences, Nursing, or Pharmacy with monitoring experience.

The predicted salary is between 36000 - 60000 £ per year.

A leading clinical research organization in London is seeking a Clinical Research Compliance Manager to oversee compliance with clinical procedures and ensure data integrity in adherence to ICH GCP guidelines. This role includes managing external monitoring visits, training staff on compliance matters, and implementing quality assurance programs.

The ideal candidate has a BSc or higher in Life Sciences, Nursing, or Pharmacy and proven experience in monitoring clinical data. Opportunities for competitive salary and benefits are provided.

Strategic Clinical Research Compliance Lead employer: Richmond Pharmacology

As a leading clinical research organisation based in London, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee growth and development. Our commitment to excellence is reflected in our competitive salary packages, comprehensive benefits, and opportunities for professional advancement, making us an exceptional employer for those passionate about making a meaningful impact in the field of clinical research.
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Contact Detail:

Richmond Pharmacology Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Strategic Clinical Research Compliance Lead

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a job that’s perfect for you.

✨Tip Number 2

Prepare for interviews by brushing up on ICH GCP guidelines and compliance procedures. We want you to be the go-to expert in the room, so practice answering questions related to data integrity and quality assurance.

✨Tip Number 3

Don’t just apply anywhere; focus on organisations that align with your values and career goals. Check out our website for openings that match your skills and interests, and tailor your approach to each one.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can set you apart from other candidates. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.

We think you need these skills to ace Strategic Clinical Research Compliance Lead

Clinical Research Compliance
Data Integrity
ICH GCP Guidelines
External Monitoring Management
Staff Training
Quality Assurance Programs
Monitoring Clinical Data
Life Sciences Knowledge
Nursing Knowledge
Pharmacy Knowledge
Analytical Skills
Attention to Detail
Communication Skills
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical research and compliance. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills and achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research compliance and how your expertise can benefit us at StudySmarter. Keep it engaging and to the point!

Showcase Your Knowledge of ICH GCP Guidelines: Since this role involves ensuring adherence to ICH GCP guidelines, make sure to mention any specific experiences or training you have related to these standards. We love candidates who are well-versed in compliance matters!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves!

How to prepare for a job interview at Richmond Pharmacology

✨Know Your ICH GCP Guidelines

Make sure you brush up on the ICH GCP guidelines before your interview. Being able to discuss these in detail will show that you understand the compliance landscape and can effectively oversee clinical procedures.

✨Showcase Your Monitoring Experience

Prepare specific examples from your past roles where you successfully monitored clinical data. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and experience in the field.

✨Prepare for Compliance Scenarios

Think about potential compliance scenarios that could arise in clinical research. Be ready to discuss how you would handle these situations, as it shows your proactive approach and understanding of quality assurance programs.

✨Engage with Questions

Have a few thoughtful questions ready to ask the interviewer about their compliance processes and team dynamics. This not only shows your interest in the role but also helps you gauge if the company is the right fit for you.

Strategic Clinical Research Compliance Lead
Richmond Pharmacology
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