Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical projects, ensuring timely delivery and compliance with regulations.
- Company: Dynamic clinical research organisation based in Central London.
- Benefits: Competitive salary, professional development, and a chance to work on impactful studies.
- Why this job: Join a global network and make a difference in healthcare through innovative clinical trials.
- Qualifications: 5-10 years of clinical project management experience and strong regulatory knowledge.
- Other info: Opportunity for career growth in a fast-paced, collaborative environment.
The predicted salary is between 48000 - 72000 £ 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 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
✨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 engage with others, the better your chances of hearing about job openings that might not even be advertised.
✨Show Off Your Skills
When you get the chance to chat with potential employers, don’t hold back! Share specific examples of how you've successfully managed projects, especially in cardiovascular or oncology studies. We want to see your expertise shine through!
✨Follow Up After Interviews
After an interview, drop a quick thank-you email to express your appreciation for the opportunity. It’s a simple gesture that keeps you on their radar and shows your enthusiasm for the role. Plus, it gives you a chance to reiterate why you’re the perfect fit!
✨Apply Through Our Website
Don’t forget to check out our website for the latest job openings! Applying directly through us can sometimes give you an edge, as we’re always looking for passionate candidates who are ready to make an impact in clinical project management.
We think you need these skills to ace Clinical Project Manager - Site Initiation
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in clinical project management, especially in study start-up and regulatory affairs. We want to see how your skills align with the role, so don’t be shy about showcasing your relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Clinical Project Manager position. Mention your experience with cardiovascular studies and how you can contribute to our team’s success.
Showcase Your Communication Skills: Since strong communication is key in this role, make sure your application reflects that. Use clear and concise language, and don’t forget to proofread for any typos or errors. We appreciate attention to detail!
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’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!
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 the areas of cardiovascular, haematology, and oncology. Familiarise yourself with ICH-GCP guidelines and be ready to discuss how you've applied them in your previous roles.
✨Showcase Your Experience
Prepare specific examples from your past work that highlight your experience in site initiation and contract negotiation. Be ready to explain how you managed timelines and vendors effectively, 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 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 and values.