
1 - 10 employees
Founded 2017
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $100M Private Equity Round on 2022-04
Healthcare • Biotechnology • Pharmaceuticals
Dianthus Therapeutics, Inc. is a clinical-stage biotechnology company focused on developing novel monoclonal antibodies to treat severe autoimmune and inflammatory diseases. The company leverages advanced antibody engineering technologies to create next-generation complement therapeutics with improved selectivity and potency. Its lead program, DNTH103, is a monoclonal antibody targeting the classical complement pathway for conditions such as generalized Myasthenia Gravis, Multifocal Motor Neuropathy, and Chronic Inflammatory Demyelinating Polyneuropathy. Based in New York City and Waltham, Massachusetts, Dianthus aims to deliver transformative medicinal therapies by addressing unmet needs in autoimmune treatment.
🕒 July 30
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1 - 10 employees
Founded 2017
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $100M Private Equity Round on 2022-04
Healthcare • Biotechnology • Pharmaceuticals
Dianthus Therapeutics, Inc. is a clinical-stage biotechnology company focused on developing novel monoclonal antibodies to treat severe autoimmune and inflammatory diseases. The company leverages advanced antibody engineering technologies to create next-generation complement therapeutics with improved selectivity and potency. Its lead program, DNTH103, is a monoclonal antibody targeting the classical complement pathway for conditions such as generalized Myasthenia Gravis, Multifocal Motor Neuropathy, and Chronic Inflammatory Demyelinating Polyneuropathy. Based in New York City and Waltham, Massachusetts, Dianthus aims to deliver transformative medicinal therapies by addressing unmet needs in autoimmune treatment.
• You will oversee all clinical data management activities and deliverables from study start-up through database lock and closeout across multiple clinical trials. • Working independently with cross-functional teams and external partners, you will ensure the delivery of complete, accurate, high-quality, and regulatory-compliant data to support study reporting, publications, and regulatory submissions. • This role requires a balance of strong operational execution and innovative thinking to advance data quality, integration, and analysis in support of clinical development goals.
• Bachelors degree in life sciences required • Minimum of 5 years of clinical data management experience in Sponsor and/or CRO setting • Strong understanding of DM related systems, technologies and standards including data analytics platforms • Comprehensive knowledge of drug development and clinical research processes, GCP guidelines and regulations related to clinical data management • Self-motivated and able to work autonomously as well as take direction and work within a high-functioning and collaborative team environment • Detail-oriented with strong verbal and written communication skills • Ability to build relationships internally and with external partners • Highest levels of professionalism, confidence, personal values and ethical standards.
• We are open to you working remotely.
Apply Now🕒 July 30
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