Director, Project Management at Dianthus Therapeutics

We are a clinical-stage biotechnology company dedicated to developing transformative therapies for patients suffering from severe autoimmune diseases. Our pipeline includes innovative candidates like claseprubart, which is designed for high selectivity and patient convenience through subcutaneous delivery, and our bifunctional inhibitor, DNTH212, which targets multiple disease-modifying mechanisms. We are currently looking for a Director of Project Management to join our team and help us advance these critical programs. This is a full-time, remote position that offers you the opportunity to work alongside scientific leaders to shape our drug development strategy and improve patient outcomes.

Key outcomes

• Collaborate with scientific leadership to define and execute the strategic objectives and work plans for your assigned programs.
• Create and manage integrated program plans, including detailed timelines, resource allocation, and budget tracking.
• Facilitate cross-functional communication and decision-making to ensure all program activities remain aligned with our corporate goals.
• Identify potential risks and operational bottlenecks early, developing effective mitigation strategies to keep projects on schedule.
• Partner with our finance team and scientific staff to build and monitor comprehensive program budgets.
• Develop clear, impactful presentations that distill complex scientific information into actionable insights for stakeholders.
• Drive organizational efficiency by standardizing processes and identifying opportunities for continuous improvement across our R&D teams.

Requirements

• A Bachelor’s degree in any discipline is required.
• At least 9 years of program management experience within the biomedical or biopharma industry.
• A minimum of 8 years of experience in clinical development, covering the spectrum from candidate selection through Phase 1 to 3 trials and regulatory filings.
• At least 3 years of hands-on experience using tools such as MS Project, MS Excel, SharePoint, PowerPoint, and MS Word.
• Strong business acumen and the ability to foster professional relationships with both internal teams and external partners.
• Excellent communication skills and a high level of attention to detail regarding reporting and documentation.
• Fluency in English.

Preferred qualifications

• An advanced degree, such as an MS, PhD, or MBA, specifically in the Life Sciences.
• Direct experience with biologics or antibody therapy development.
• A current PMP certification.
• In-depth knowledge of US FDA and EU EMA regulations, as well as ICH guidelines for biologic products.

Compensation

We are pleased to offer a remote work environment that supports flexibility and work-life balance.

How to apply

If you are interested in contributing to our mission of elevating patient care, please submit your application through our official career portal. We look forward to reviewing your background and discussing how your experience aligns with our goals.