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.
- Other info: Opportunity for career growth in a fast-paced, collaborative environment.
- 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.
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
Join a leading clinical research organisation in Central London, where you will thrive in a dynamic work culture that prioritises collaboration and innovation. With a strong focus on employee development, we offer numerous growth opportunities and the chance to work on impactful clinical trials across various therapeutic areas, including cardiovascular, haematology, and oncology. Our commitment to excellence and compliance ensures that you will be part of a team dedicated to advancing healthcare while enjoying the benefits of working in a vibrant city.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Manager - Site Initiation
✨Unlock Networking Opportunities
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Coronado Research.
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If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Coronado Research. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
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We think you need these skills to ace Clinical Project Manager - Site Initiation
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Coronado Research!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Coronado Research that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Coronado Research!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Coronado Research, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Coronado Research
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Coronado Research that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Coronado Research’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
