Regulatory Scientist

3 weeks ago


United Kingdom Barrington James Full time

Company Overview: We are a leading biopharmaceutical company dedicated to advancing the field of cell metabolism and developing innovative therapies across oncology and inflammation. Our mission is to transform patient care through the discovery and development of groundbreaking treatments that target key pathways of the immune system.
Lead the design and implementation of phase I clinical trials (and later as programs progress) in various indications, with a focus on immunometabolic pathways.
# Collaborate with cross-functional teams to develop and execute clinical development plans, ensuring alignment with corporate goals and regulatory requirements.
# Provide scientific expertise and guidance on trial design, protocol development, and patient selection criteria.
# Oversee the collection, analysis, and interpretation of clinical trial data, including safety, efficacy, and pharmacokinetic/pharmacodynamic endpoints.
# Prepare clinical study reports, regulatory submissions, and presentations for internal and external stakeholders.
# Interface with key opinion leaders, clinical investigators, and regulatory authorities to support the successful execution of clinical trials.
# Stay abreast of emerging scientific literature, technological advancements, and competitive landscape in immunometabolism and dermatology.


PhD or equivalent degree in immunometabolism, immunology, or a related field.
# Minimum of 3-10 years of industry experience in clinical research, with a strong track record of success in playing a key role in dermatology trials.
# Demonstrated ability to work effectively in cross-functional teams and manage multiple projects simultaneously.
# Excellent communication and presentation skills, with the ability to communicate complex scientific concepts clearly and persuasively.
# Strong analytical skills and proficiency in data analysis and interpretation.
#



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