Manager, Regulatory Clinical Applications

November 24

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Dianthus Therapeutics, Inc.

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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.

2 - 10 employees

Founded 2017

🧬 Biotechnology

💊 Pharmaceuticals

💰 $100M Private Equity Round on 2022-04

📋 Description

• Support the Director in coordinating and implementing study startup activities in collaboration with CROs and internal study teams. • Assist in identifying country-specific regulatory and ethics committee requirements to facilitate timely CTA approvals. • Review and prepare submission packages for Regulatory Authorities and IRB/IEC for completeness and accuracy. • Ensure required Quality documentation (e.g., QP declaration, GMP Certification) is available for drug release. • Track and coordinate responses to Regulatory and IRB/IEC queries and deficiency letters with subject matter experts. • Monitor and report on CTA status updates and study startup progress across assigned projects. • Maintain internal regulatory files and ensure documentation is complete and accessible. • Support the review and maintenance of the Trial Master File for regulatory and ethics committee documentation. • Update global clinical trial registries (e.g., ClinicalTrials.gov) as required. • Participate in Study Management Team meetings to represent regulatory/study startup perspectives. • Assist in gathering and sharing regulatory intelligence related to study startup. • Contribute to the development and maintenance of SOPs and process improvement initiatives. • Support strategic planning and risk mitigation efforts related to study startup activities. • Travel up to 10% for team meetings and company events.

🎯 Requirements

• 5+ years of experience in clinical trial startup and regulatory affairs within the pharmaceutical or biotech industry. • Bachelor’s degree in life sciences or related field required; advanced degree preferred. • Familiarity with CRO operations and global regulatory requirements for clinical trial applications. • Experience supporting global interventional clinical studies and managing CTA submissions. • Strong organizational skills with the ability to manage multiple priorities and meet deadlines. • Knowledge of GxP, ICH guidelines, and health authority regulations. • Effective communication and interpersonal skills; ability to work collaboratively across teams. • Detail-oriented with strong analytical and problem-solving capabilities. • Proficiency in project management and documentation systems.

🏖️ Benefits

• Health insurance • 401(k) plan • Paid time off • Professional development opportunities