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Medical Director

DermBiont, Inc.

This is a Full-time position in Emeryville, CA posted July 6, 2021.

Organization: DermBiont?s mission is to become the world?s leading precision dermatology company developing targeted topical therapeutics that treat, cure, and prevent diseases.

The company aims to impact the root cause of skin diseases with biotherapeutics that repair an imbalance of the microbiome as well as through the development of targeted small molecule therapeutics with well-defined mechanisms of action.

DermBiont?s biotherapeutics discovery team leverages computational biology and a proprietary bioinformatics platform to identify clinically meaningful dysbiosis related to common skin diseases and mines a curated library of microbes to build a pipeline of products to treat identified dysbiosis across indications.

Key responsibilities: * Work with key internal and external stakeholders to design and implement clinical trials in support of our clinical development plans through providing medical and clinical expertise and oversight* Be medical monitor of clinical trials* Design and draft protocol synopses, clinical trial protocols and protocol amendments* Writing of IBs, study protocols, regulatory documents, CSRs and publications associated with the clinical trials* Provide medical input and guidance on scientific, clinical and safety monitoring issues* Maintain scientific and clinical knowledge in the relevant therapeutic and disease area(s)* Act as a medical/clinical representative in cross-functional teams and meetings* Assist in the development of patient-oriented materials and educational tools Qualifications: * Medical Degree* Experience in dermatology and/or infectious diseases a plus but not required* Strong writings skills essential / experience writing protocols preferred* Clinical development experience and/or clinical trial experience desirable.* Basic knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in development of clinical strategy and the design of study protocols* A history of strong collaboration and personal interaction with all levels of internal stakeholders including, Regulatory Affairs, Medical Affairs, Clinical Operations, Biometrics, Research, Preclinical Science and Product Development* Strong interpersonal, presentation, written and verbal communication skills* Demonstrated managerial skills as it relates to training, listening, empowering, coaching, and delivering feedback* Preferred: Experience in clinical development biotechnology/pharmaceutical industrial setting preferred