At a Glance
- Tasks: Manage global clinical trials and lead project planning for new studies.
- Company: Dynamic pharmaceutical company focused on innovative clinical solutions.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Join a collaborative team with a focus on continuous improvement and global impact.
- Why this job: Make a real impact in healthcare by overseeing critical clinical trials.
- Qualifications: Experience in pharmaceutical clinical trials and strong project management skills.
The predicted salary is between 48000 - 72000 £ per year.
The Senior Clinical Project Manager (sCPM) is responsible for the end-to-end operational management and oversight of pharmaceutical clinical trials within a global program. This is a hands-on execution role that requires the ability to manage the day-to-day delivery of clinical trials while contributing to high-level lifecycle management discussions and program strategy.
The successful candidate will support an existing study team on an ongoing global program while also taking the lead on new studies. This role acts as a key link within the Clinical Operations department, ensuring seamless delivery across the clinical development lifecycle from pre-clinical stages all the way through.
Responsibilities
- Lead the end-to-end operational management of pharmaceutical clinical trials, with a focus on a global multi-centre Phase IIa study in Pancreatic Insufficiency.
- Lead the planning and preparation for upcoming Phase IIb and Phase III transitions, ensuring all operational requirements are lined up for the next phases.
- Take full ownership of a confidential Phase I study within the same program, managing it from startup through to completion.
- Provide high-level oversight of the clinical development lifecycle, including participating in lifecycle management (LCM) discussions.
- Deliver hands-on project management, supporting existing Project Managers while simultaneously running independent studies.
- Oversee CROs and external vendors to ensure delivery to timelines, budget, and quality standards.
- Facilitate collaboration across global functions to drive inspection readiness and continuous improvement.
Qualifications & Experience
- Relevant pharmaceutical clinical trial experience (Pharma, Biotech, or CRO).
- Proven experience in Pharmaceutical studies is essential (Nutritional study experience is a plus but Pharma background is the priority).
- Extensive experience across the full trial lifecycle, specifically moving studies from Phase II into Phase III.
- Strong experience in Global Multi-centre study management.
- Proficient in ICH-GCP, CFR, and applicable regulatory guidelines.
Logistics & Travel
- Work Pattern: Remote with a link to the London (Victoria) hub.
- Travel: Approximately 20% travel required, including quarterly meetings in London and travel to Switzerland as necessary.
Senior Clinical Project Manager in London employer: Randstad UK
Randstad UK is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of Manchester. With a strong focus on employee development through comprehensive learning and development training, as well as access to cutting-edge recruitment technology, we empower our team to excel and achieve their career goals while enjoying the benefits of uncapped earning potential in a thriving sector.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Project Manager in London
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We think you need these skills to ace Senior Clinical Project Manager in London
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 Randstad UK!
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 Randstad UK 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 Randstad UK!
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 Randstad UK, 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 Randstad UK
✨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 Randstad UK 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 Randstad UK’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.
