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For Companies At a Glance
- Tasks: Lead clinical studies in ophthalmology, focusing on retinal diseases and developing key clinical documents.
- Company: Join a growing, well-funded company dedicated to advancing treatments for ophthalmic diseases.
- Benefits: Enjoy remote work flexibility and competitive salary based on your expectations.
- Why this job: Be part of impactful early-phase clinical development in a supportive and innovative environment.
- Qualifications: Must be a board-certified ophthalmologist with industry experience in CRO, Pharma, or Biotech.
- Other info: Ideal candidates should have experience in Phase I-II and preferably Phase III clinical trials.
The predicted salary is between 72000 - 108000 £ per year.
Ophthalmologist, Clinical Development – Permanent:
Location: UK or EU Remote
Salary/Compensation: Based on candidate expectations.
The Role:
– \”Board Certified\” Ophthalmologist, specialising in Retinal diseases
– Looking for someone with some industry experience in CRO, Pharma, Biotech
– Should have experience with authoring/developing Clinical Development Plans, Protocols and other key clinical documentation (IB\’s, ICF\’s etc.).
– Someone to serve as MD Clinical Lead for the study.
– Early development (Phase I-II) a MUST, really hoping for Phase III as well if possible.
The Company:
Our client are a growing company, circa 40 headcount currently across Europe and the USA, they\’re well-funded and are focused on the development of Ophthalmic diseases.
Clinical Development Ophthalmologist employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Development Ophthalmologist
✨Tip Number 1
Make sure to highlight your experience in clinical development, especially in early phases like Phase I and II. If you have any involvement in Phase III studies, be sure to mention that as well, as it’s a key requirement for this role.
✨Tip Number 2
Network with professionals in the CRO, Pharma, and Biotech industries. Attend relevant conferences or webinars where you can connect with others in the field and potentially get referrals or insights about the company.
✨Tip Number 3
Familiarize yourself with the latest trends and developments in retinal diseases. Being knowledgeable about current research and advancements will not only help you in interviews but also show your passion for the field.
✨Tip Number 4
Prepare to discuss your experience with authoring clinical documentation like Clinical Development Plans and Protocols. Be ready to provide examples of how your contributions have positively impacted previous studies.
We think you need these skills to ace Clinical Development Ophthalmologist
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your experience as a board-certified ophthalmologist, particularly in retinal diseases. Mention any previous roles in CRO, Pharma, or Biotech that relate to clinical development.
Detail Your Clinical Documentation Skills: Clearly outline your experience with authoring and developing Clinical Development Plans, Protocols, and other key clinical documentation such as Investigator's Brochures (IBs) and Informed Consent Forms (ICFs).
Showcase Early Development Experience: Since early development experience (Phase I-II) is a must, be sure to provide specific examples of your involvement in these phases. If you have experience in Phase III, highlight that as well.
Tailor Your Application: Customize your CV and cover letter to reflect the specific requirements mentioned in the job description. Use keywords from the job listing to demonstrate that you are a perfect fit for the role.
How to prepare for a job interview at Planet Pharma
✨Showcase Your Clinical Expertise
Make sure to highlight your experience as a board-certified ophthalmologist, especially in retinal diseases. Be prepared to discuss specific cases or studies you've worked on that demonstrate your clinical knowledge and skills.
✨Discuss Your Industry Experience
Since the role requires some industry experience in CRO, Pharma, or Biotech, be ready to talk about your previous roles in these settings. Share examples of how you contributed to clinical development plans and protocols.
✨Prepare for Technical Questions
Expect questions related to authoring key clinical documentation such as Investigator's Brochures (IBs) and Informed Consent Forms (ICFs). Brush up on your knowledge of these documents and be ready to explain your process for developing them.
✨Emphasize Early Development Experience
Since early development (Phase I-II) experience is a must, prepare to discuss your involvement in these phases. If you have experience with Phase III trials, make sure to mention it as well, as it will strengthen your candidacy.
