Arvinas
Senior Director, Clinical Scientist - Neuroscience
Remote, Hybrid, New Haven - CT Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its PROTACDiscovery Engine platform to engineer proteolysis targeting chimeras (PROTACs) that degrade disease-causing proteins. In addition to its robust preclinical PROTAC pipeline, the company has three investigational clinical-stage programs enrolling: ARV-102 for neurodegenerative disorders, ARV-393 for relapsed/refractory non-Hodgkin lymphoma and potentially other lymphomas, and ARV-806, a KRAS G12D PROTAC for solid tumors with KRAS G12D mutations. This role supports Global Clinical Development in neuroscience-focused programs and related activities. This position reports to the Head of Clinical Sciences and can be hybrid at our headquarters in New Haven, CT, or remote from a location within the U.S. Responsibilities
Provide scientific support for Global Clinical Development activities, assembling, evaluating, and presenting scientific and medical data. Write or contribute content to clinical documents (clinical study protocols and protocol synopses, papers, abstracts, posters, etc.). Monitor the competitive landscape and summarize relevant literature to provide strategic input. Collaborate with Clinical Operations, Translational Sciences, Clinical Pharmacology, Regulatory, Research and other functions within Arvinas, as well as key external partners. Collaborate on the development of clinical documents and data communications for internal and external audiences. Study/Technical Focus
Clinical Document Development Clinical Study Planning Study Data Review and Analysis Review of Scientific Literature Qualifications
Required: Advanced doctoral degree (PhD, MD, MSc/MPH, PharmD) or equivalent professional experience. 10+ years of experience in a pharmaceutical company environment. Neurodegenerative/neuromuscular disease experience or educational background. Advanced knowledge of GCP/ICH, drug development process, study design, statistics, and clinical operations in the neurodegenerative/neuromuscular setting. Excellent project management, communication, and organizational skills with demonstrated success in leading projects and cross-functional collaboration. Ability to work independently and deliver high-quality work on time. Clear written and verbal communication to scientific and medical audiences. Arvinas will not be providing VISA sponsorship for this position now or in the future. You must have the ability to work without a need for current or future VISA sponsorship. Equal Opportunity
Arvinas is an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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Remote, Hybrid, New Haven - CT Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its PROTACDiscovery Engine platform to engineer proteolysis targeting chimeras (PROTACs) that degrade disease-causing proteins. In addition to its robust preclinical PROTAC pipeline, the company has three investigational clinical-stage programs enrolling: ARV-102 for neurodegenerative disorders, ARV-393 for relapsed/refractory non-Hodgkin lymphoma and potentially other lymphomas, and ARV-806, a KRAS G12D PROTAC for solid tumors with KRAS G12D mutations. This role supports Global Clinical Development in neuroscience-focused programs and related activities. This position reports to the Head of Clinical Sciences and can be hybrid at our headquarters in New Haven, CT, or remote from a location within the U.S. Responsibilities
Provide scientific support for Global Clinical Development activities, assembling, evaluating, and presenting scientific and medical data. Write or contribute content to clinical documents (clinical study protocols and protocol synopses, papers, abstracts, posters, etc.). Monitor the competitive landscape and summarize relevant literature to provide strategic input. Collaborate with Clinical Operations, Translational Sciences, Clinical Pharmacology, Regulatory, Research and other functions within Arvinas, as well as key external partners. Collaborate on the development of clinical documents and data communications for internal and external audiences. Study/Technical Focus
Clinical Document Development Clinical Study Planning Study Data Review and Analysis Review of Scientific Literature Qualifications
Required: Advanced doctoral degree (PhD, MD, MSc/MPH, PharmD) or equivalent professional experience. 10+ years of experience in a pharmaceutical company environment. Neurodegenerative/neuromuscular disease experience or educational background. Advanced knowledge of GCP/ICH, drug development process, study design, statistics, and clinical operations in the neurodegenerative/neuromuscular setting. Excellent project management, communication, and organizational skills with demonstrated success in leading projects and cross-functional collaboration. Ability to work independently and deliver high-quality work on time. Clear written and verbal communication to scientific and medical audiences. Arvinas will not be providing VISA sponsorship for this position now or in the future. You must have the ability to work without a need for current or future VISA sponsorship. Equal Opportunity
Arvinas is an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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