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For Companies At a Glance
- Tasks: Manage clinical studies, budgets, and timelines while collaborating with diverse teams.
- Company: Leading medical device company focused on innovative cardiovascular solutions.
- Benefits: Attractive salary, comprehensive health benefits, and a supportive work environment.
- Why this job: Join a dynamic team making a real difference in healthcare through cutting-edge projects.
- Qualifications: Bachelor's degree in health sciences and 2 years of clinical project management experience required.
- Other info: Exciting opportunities for career growth in a fast-paced industry.
The predicted salary is between 90000 - 105000 £ per year.
Responsibilities
- Manage clinical study timelines and budgets, including vendor selection and contract oversight.
- Facilitate communication among cross‑functional teams (R&D, Regulatory, Marketing) and investigational sites.
- Oversee regulatory submissions and ensure compliance with ISO and local regulations.
- Provide input on protocol design, case report forms, and monitoring plans.
- Coordinate investigator meetings, steering committees, and study‑specific training for internal and site personnel.
Qualifications
- Minimum of a Bachelor's degree in health sciences or related field.
- At least 2 years of clinical project management experience; cardiovascular or cardiology device experience strongly preferred.
- Proven ability to manage study budgets and timelines effectively.
- Strong knowledge of ISO standards and clinical trial regulations.
- Excellent communication, organizational, and leadership skills; proficiency in project management tools and Microsoft Office Suite.
Compensation
- Salary: $125,000-$145,000 / year (USD)
- Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K.
Application Details
- This job opens for applications on 12 / 17 / 25.
- Applications for this job will be accepted for at least 30 days from the posting date.
Keywords
- clinical project management
- clinical trials
- medical device
- cardiology
- GCP
- ISO compliance
- regulatory submissions
- budgeting
- vendor management
- protocol design
- cross‑functional collaboration
- project timelines
- investigator meetings
- clinical operations
Clinical Project Manager in Plymouth employer: Piper Companies
Contact Detail:
Piper Companies Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Project Manager in Plymouth
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical project management field. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO standards and clinical trial regulations. We recommend creating a list of common interview questions related to project management and practising your responses. Confidence is key!
✨Tip Number 3
Showcase your organisational skills! During interviews, share specific examples of how you’ve managed study budgets and timelines effectively. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search. Let’s get you that Clinical Project Manager role!
We think you need these skills to ace Clinical Project Manager in Plymouth
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your clinical project management experience, especially in cardiovascular or cardiology devices. We want to see how your skills align with the job description, so don’t be shy about showcasing relevant projects you've managed.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how your background makes you a perfect fit for our team. We love hearing personal stories that connect your experience to the role.
Showcase Your Communication Skills: Since this role involves facilitating communication among various teams, make sure to highlight your communication skills in your application. We appreciate clear and concise writing, so keep it professional yet approachable!
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 gives you a chance to explore more about what we do at StudySmarter!
How to prepare for a job interview at Piper Companies
✨Know Your Stuff
Make sure you brush up on clinical project management principles, especially around budgeting and timelines. Familiarise yourself with ISO standards and local regulations, as these will likely come up in conversation.
✨Showcase Your Experience
Be ready to discuss your previous roles in managing clinical studies, particularly in cardiology or cardiovascular devices. Prepare specific examples that highlight your ability to manage budgets and timelines effectively.
✨Communication is Key
Since the role involves facilitating communication among cross-functional teams, practice articulating how you've successfully collaborated with R&D, Regulatory, and Marketing teams in the past. Highlight any experience coordinating investigator meetings or training sessions.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical trials and their expectations for the role. This shows your genuine interest and helps you assess if the company aligns with your career goals.
