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For Companies At a Glance
- Tasks: Lead post-market clinical research in ophthalmology, managing trials and collaborating with teams.
- Company: Join a top global healthcare manufacturer focused on innovative vision-improving products.
- Benefits: Enjoy remote work flexibility or a permanent hybrid role with a dynamic team.
- Why this job: Make a real impact in healthcare while working with cutting-edge technology and research.
- Qualifications: Must have a higher degree in Optometry/Ophthalmology or significant related experience.
- Other info: Equal Opportunity Employer; we support diverse applicants and provide interview assistance.
The predicted salary is between 43200 - 72000 £ per year.
Contract – Senior Clinical Trial Scientist – Medical Device Company – Remote
PLEASE NOTE THIS ROLE IS ALSO AVAILABLE AS A PERMANENT HYBRID ROLE.
Further details can be found via www.carrotrecruitment.co.uk
The Company
Carrot Recruitment are partnered with a leading global manufacturer in the healthcare industry, specializing in innovative products that improve vision and quality of life. With a strong commitment to research and development, the company is at the forefront of technological advancements in its field.
The Role
As part of their dynamic team, you\’ll be responsible for the planning and management of post-market clinical research primarily within the UK and then spanning into Europe. Part of your role will include:
- Writing and reviewing protocols and related study materials
- Obtaining ethics approval, writing informed consent documentation
- Maintenance of existing trials and management/setup of new trial and sites.
- Oversee study execution, working in collaboration with the clinical operation team.
- Perform or oversee statistical analysis and write /review study reports
- Work in accordance to industry regulations and maintain up to date knowledge of these regulations at all time, ensuring any changes are implemented accordingly.
You
- Hold a Higher Clinical/Research/Scientific Degree (ideally in Optometry/Ophthalmology) or significant experience of working in the area of ophthalmology/proven enhanced knowledge to act as a SME.
- Have experience of working in the medical device industry and experience in clinical trials at later phase to post-marketing stages ideally
- Be experienced in clinical trial design, site feasibility, statistical analysis, creation of protocols, medical writing, clinical research ethics and regulatory knowledge.
- Excellent communication skills with key stakeholders and KOLs (ideally in the specified field of Ophthalmology)
What should you do next?
To discuss this role further or to find out about other roles I’m currently working on, 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.
Senior Clinical Trial Scientist (Ophthalmology) employer: Carrot Recruitment
Contact Detail:
Carrot Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Trial Scientist (Ophthalmology)
✨Tip Number 1
Make sure to highlight your experience in ophthalmology and clinical trials during networking events or discussions. Engaging with professionals in the field can lead to valuable connections and insights about the role.
✨Tip Number 2
Stay updated on the latest advancements in ophthalmology and medical devices. This knowledge will not only help you in interviews but also demonstrate your passion for the field and commitment to continuous learning.
✨Tip Number 3
Prepare to discuss specific examples of your previous work in clinical trial management, especially related to post-market studies. Being able to articulate your contributions and outcomes will set you apart from other candidates.
✨Tip Number 4
Familiarize yourself with the regulatory landscape in the UK and Europe regarding clinical trials. Showing that you understand these regulations will demonstrate your readiness to navigate the complexities of the role.
We think you need these skills to ace Senior Clinical Trial Scientist (Ophthalmology)
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Senior Clinical Trial Scientist position. Understand the key responsibilities, required qualifications, and the specific skills needed in ophthalmology and clinical trials.
Tailor Your CV: Customize your CV to highlight relevant experience in clinical trials, particularly in the medical device industry and ophthalmology. Emphasize your skills in protocol writing, statistical analysis, and regulatory knowledge.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for ophthalmology and your experience in managing clinical trials. Mention specific achievements and how they align with the company's commitment to innovation in healthcare.
Highlight Communication Skills: Since excellent communication skills are crucial for this role, provide examples in your application of how you've effectively communicated with stakeholders and KOLs in previous positions.
How to prepare for a job interview at Carrot Recruitment
✨Showcase Your Expertise in Ophthalmology
Make sure to highlight your knowledge and experience in ophthalmology during the interview. Be prepared to discuss specific projects or trials you've worked on, especially those related to medical devices.
✨Demonstrate Your Understanding of Clinical Trial Processes
Familiarize yourself with the entire clinical trial process, particularly post-market studies. Be ready to explain how you have contributed to protocol writing, ethics approval, and trial management in your previous roles.
✨Communicate Effectively with Stakeholders
Since excellent communication skills are crucial for this role, practice articulating your thoughts clearly. Prepare examples of how you've successfully collaborated with key stakeholders and KOLs in past projects.
✨Stay Updated on Industry Regulations
Research the latest regulations in clinical trials and medical devices. Be prepared to discuss how you ensure compliance and adapt to changes in regulations within your work.
