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- Tasks: Lead clinical projects, ensuring compliance and effective communication across teams.
- Company: Dynamic clinical research organisation with a global network.
- Benefits: Competitive salary, professional development, and a vibrant work environment.
- Why this job: Make a real difference in healthcare by managing impactful clinical trials.
- Qualifications: 5-10 years in clinical project management with strong regulatory experience.
- Other info: Opportunity to work on diverse therapeutic areas, including cardiovascular and oncology.
The predicted salary is between 36000 - 60000 £ per year.
We are urgently seeking a Clinical Project Manager who is able to work on-site in Central London with expertise in study start up, site contract negotiation as well as clinical project management. Our client has an extensive global network of sites they work with to provide clinical trials to a range of sponsors and across various therapeutic areas, although there is a focus on cardiovascular, haematology and oncology therapeutic areas. Ideally, we are seeking a CMP with a minimum of three years' experience in the role - someone who can quickly adapt and provide effective support to the team in the background. Strong regulatory affairs experience (e.g., submissions) is essential.
Responsibilities
- Provide short-term project management support to an ongoing clinical study, ensuring delivery within agreed timelines, budgets, and quality standards, in full compliance with ICH-GCP, SOPs, and regulatory requirements.
- Oversee study operations and vendors, including CROs, sites, and external partners, maintaining effective communication, risk management, and documentation (e.g., TMF, contracts, budgets, and reports).
- Support the Clinical Operations team with coordination, issue resolution, and preparation of key study materials, contributing to process improvement and ensuring continuity during team absences.
Qualifications
- 5-10 years of overall clinical project management experience within a CRO or sponsor environment.
- Proven ability to manage timelines, vendors, and multi-site studies in accordance with ICH-GCP.
- Strong communication, organizational, and problem-solving skills; experience in cardiovascular studies preferred.
- Solid experience in regulatory affairs (submissions and documentation).
- Global experience managing complex interventional and observational studies.
Clinical Project Manager - Site Initiation in London employer: Coronado Research
Contact Detail:
Coronado Research Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Project Manager - Site Initiation in London
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, workshops, or even local meet-ups. The more you mingle, the better your chances of landing that Clinical Project Manager role.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience in study start-up and regulatory affairs. We want them to see how your background fits perfectly with their needs!
✨Follow Up After Interviews
Don’t just leave it after the interview! Shoot them a quick thank-you email, reiterating your interest in the role and why you’re a great fit. It shows enthusiasm and keeps you on their radar.
✨Apply Through Our Website
We’ve got loads of opportunities listed on our website, so don’t miss out! Applying directly through us can give you an edge, as we know what our clients are looking for in a Clinical Project Manager.
We think you need these skills to ace Clinical Project Manager - Site Initiation in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Project Manager role. Highlight your experience in study start-up, site contract negotiation, and any relevant therapeutic areas like cardiovascular or oncology. We want to see how your background fits with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention your regulatory affairs experience and how you’ve successfully managed timelines and vendors in past projects. Let us know what makes you tick!
Showcase Your Communication Skills: As a Clinical Project Manager, strong communication is key. In your application, give examples of how you've effectively communicated with teams, vendors, and stakeholders. We love seeing candidates who can keep everyone on the same page!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates. Plus, it’s super easy to do!
How to prepare for a job interview at Coronado Research
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical project management, especially in cardiovascular, haematology, and oncology areas. Familiarise yourself with ICH-GCP guidelines and be ready to discuss how you've applied them in past projects.
✨Showcase Your Experience
Prepare specific examples from your previous roles that highlight your experience in site initiation and contract negotiation. Be ready to explain how you managed timelines and vendor relationships, as well as any challenges you faced and how you overcame them.
✨Communication is Key
Since strong communication skills are essential for this role, practice articulating your thoughts clearly and concisely. Think about how you can demonstrate your ability to maintain effective communication with CROs, sites, and external partners during the interview.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's current projects and their approach to clinical trials. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.