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- Tasks: Lead and manage clinical trials, ensuring compliance and successful execution.
- Company: Join a global medical device company dedicated to innovation and employee growth.
- Benefits: Enjoy competitive salary, professional development opportunities, and a supportive work culture.
- Why this job: Make an impact in healthcare while mentoring a dynamic team in a fast-paced environment.
- Qualifications: Bachelor's degree in a scientific field; experience in clinical research and leadership required.
- Other info: Ophthalmology experience is a plus; remote work options may be available.
The predicted salary is between 42000 - 84000 £ per year.
A global medical device company is seeking a highly motivated and experienced Manager of Clinical Trials Operations to manage a dynamic team with both hands-on trial management and leadership experience.
The ideal candidate will have a strong background in clinical research and management, focusing on overseeing the execution of clinical trials and ensuring compliance with regulations and protocols for medical devices.
The Role
- Oversee and manage the planning and execution of PMCF studies, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Lead a team of Clinical Research Associates (CRAs).
- Collaborate with cross-functional teams to develop and implement clinical trial protocols, informed consent forms, and other study-related documents.
- Monitor and track study progress, including patient recruitment, data collection, and monitoring activities.
- Manage trial budgets, timelines, and resource allocation to ensure successful trial completion.
- Serve as the primary point of contact for study sponsors, investigators, and other stakeholders.
You
- Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred.
- Seasoned professional within clinical research, with extensive medical device exposure and expertise in clinical trial management, including protocol development, site selection, and monitoring (Ophthalmology experience desirable).
- Leadership/management experience with excellent communication skills and the ability to effectively mentor and motivate team members.
- Knowledge of regional regulatory requirements (UK & EU), GCP, and ICH guidelines. (Experience of Regulatory submission advantageous).
- Experience in the setup and management of post-market clinical follow-up (PMCF) studies.
- Vendor management (CRO oversight) experience.
This role encompasses the opportunity to work with an established medical device company with a global presence committed to employees' personal and professional development.
To discuss this role further or to find out about other roles, please get in touch or hit apply to submit your current CV.
Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.
Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.
If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.
Manager, Clinical Trial Operations employer: Carrot Recruitment
Contact Detail:
Carrot Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manager, Clinical Trial Operations
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience with medical devices. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in clinical trial operations.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines related to clinical trials in the UK and EU. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your leadership style and experiences in managing teams. Think of specific examples where you successfully mentored team members or led a project, as this will be crucial for the role.
✨Tip Number 4
Research the company’s recent projects and achievements in the medical device sector. Being knowledgeable about their work will help you tailor your conversation during interviews and show your genuine interest in the role.
We think you need these skills to ace Manager, Clinical Trial Operations
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in clinical trial management, particularly with medical devices. Emphasise any leadership roles and specific projects that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your ability to lead teams. Mention your familiarity with GCP and regulatory requirements, and how your background makes you a perfect fit for the role.
Highlight Relevant Experience: In your application, focus on your experience with PMCF studies and vendor management. Provide examples of how you've successfully managed trial budgets and timelines in previous roles.
Showcase Communication Skills: Since the role requires excellent communication skills, include examples of how you've effectively collaborated with cross-functional teams or mentored team members in your past positions.
How to prepare for a job interview at Carrot Recruitment
✨Showcase Your Clinical Expertise
Make sure to highlight your background in clinical research and management during the interview. Discuss specific experiences you've had with clinical trials, especially in medical devices, and how they relate to the role.
✨Demonstrate Leadership Skills
As this position involves leading a team of Clinical Research Associates, be prepared to share examples of how you've successfully managed and motivated teams in the past. Highlight your mentoring abilities and how you foster collaboration.
✨Understand Regulatory Requirements
Familiarise yourself with UK and EU regulatory requirements, GCP, and ICH guidelines. Be ready to discuss how you've ensured compliance in previous roles, as this is crucial for the position.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in trial management, how you overcame them, and what you learned from those experiences.
