On-Site Clinical PM: Site Initiation (London)
On-Site Clinical PM: Site Initiation (London)

On-Site Clinical PM: Site Initiation (London)

Full-Time 43200 - 72000 £ / year (est.) No home office possible
Coronado Research

At a Glance

  • Tasks: Manage clinical study operations and ensure compliance with regulations.
  • Company: Global clinical research organisation with a focus on impactful trials.
  • Benefits: Competitive salary, professional development, and the chance to make a difference.
  • Why this job: Join a dynamic team and contribute to groundbreaking cardiovascular studies.
  • Qualifications: 5-10 years of clinical project management experience and regulatory affairs expertise.
  • Other info: On-site role in central London with opportunities for career advancement.

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

A global clinical research organization is urgently seeking a Clinical Project Manager to work on-site in central London. The ideal candidate will have 5-10 years of clinical project management experience, particularly in cardiovascular studies, and strong regulatory affairs expertise.

Responsibilities include:

  • Managing study operations
  • Ensuring compliance with ICH-GCP
  • Supporting the clinical operations team

This position offers a unique opportunity to contribute to impactful clinical trials across multiple therapeutic areas.

On-Site Clinical PM: Site Initiation (London) employer: Coronado Research

As a leading global clinical research organisation, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. Located in the vibrant heart of central London, we offer competitive benefits, continuous professional development opportunities, and the chance to make a meaningful impact on healthcare through groundbreaking clinical trials. Join us to be part of a team that values your expertise and supports your growth in the dynamic field of clinical research.
Coronado Research

Contact Detail:

Coronado Research Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land On-Site Clinical PM: Site Initiation (London)

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience in cardiovascular studies. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on ICH-GCP guidelines and recent developments in clinical trials. We want you to be the go-to expert in the room, so show off that regulatory affairs knowledge!

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and match your skills, especially in impactful clinical trials.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Let’s make sure they remember you as the perfect fit for their team!

We think you need these skills to ace On-Site Clinical PM: Site Initiation (London)

Clinical Project Management
Regulatory Affairs Expertise
Study Operations Management
ICH-GCP Compliance
Cardiovascular Studies Experience
Team Support Skills
Impactful Clinical Trials Knowledge
Therapeutic Areas Understanding

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your clinical project management experience, especially in cardiovascular studies. We want to see how your skills align with the role, so don’t be shy about showcasing relevant 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 and how your background makes you a perfect fit for our team. Keep it engaging and personal – we love to see your personality!

Showcase Regulatory Knowledge: Since this role involves strong regulatory affairs expertise, make sure to mention any relevant certifications or experiences. We’re looking for someone who knows their stuff when it comes to ICH-GCP compliance!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, it shows you’re keen to join our team!

How to prepare for a job interview at Coronado Research

✨Know Your Clinical Stuff

Make sure you brush up on your clinical project management knowledge, especially in cardiovascular studies. Be ready to discuss specific projects you've managed and how you ensured compliance with ICH-GCP guidelines.

✨Showcase Your Regulatory Expertise

Since strong regulatory affairs expertise is key for this role, prepare examples of how you've navigated regulatory challenges in past projects. This will demonstrate your ability to handle the complexities of clinical trials.

✨Understand the Company’s Impact

Research the global clinical research organisation and their recent studies. Being able to articulate how your experience aligns with their mission and the impact of their work will set you apart from other candidates.

✨Prepare Questions That Matter

Think of insightful questions to ask during the interview. Inquire about their approach to managing study operations or how they support their clinical operations team. This shows your genuine interest in the role and the company.

On-Site Clinical PM: Site Initiation (London)
Coronado Research

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