Director Regulatory Affairs - Freelance

 Posted 24 days ago
     
10+ years experience
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AI Summary

Provide expert scientific and regulatory guidance for an early phase drug reformulation project in ophthalmology. Define the overall regulatory and clinical development strategy and manage interactions with European regulatory authorities.

About this role

TFS HealthScience is a leading global mid size Contract Research Organization CRO that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing, and Functional Service FSP solutions.

The Regulatory Strategy Consultant Ophthalmology is responsible for providing expert scientific and regulatory guidance on an early phase drug reformulation project, including interpretation of preclinical data and defining the optimal regulatory and clinical development strategy in Europe.

As part of our SRS FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.

This is contract position at 0.2FTE


Key Responsibilities

• Provide scientific interpretation of preclinical ophthalmology data including in vivo models to assess proof of concept
• Translate nonclinical findings into regulatory and early clinical development recommendations
• Define and guide the overall regulatory and clinical strategy for the program
• Advise on optimal next steps in development including study design and development pathway
• Support planning and execution of interactions with European regulatory authorities including scientific advice
• Recommend appropriate regulatory pathways and authority engagement strategies within Europe


Qualifications

• Bachelor’s degree in life sciences or equivalent, advanced degree preferred
• Extensive experience in regulatory affairs with a focus on early phase strategy
• Strong background in ophthalmology drug development
• Proven experience interpreting preclinical data and linking it to clinical and regulatory strategy
• Experience engaging with European regulatory authorities including scientific advice procedures


What We Offer

We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.


A Bit More About Us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a full service global CRO, we build solution driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

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