Director, Clinical Operations

Summary

Join Dianthus Therapeutics, a clinical-stage biotechnology company, as their Director, Clinical Operations. You will oversee global clinical trials, strategically direct operational planning, and implement efficient execution of programs, particularly supporting enrollment across the UK, EU, and Nordic regions for the CAPTIVATE study. This role requires strong leadership, cross-functional team management, and experience in managing external service providers. You will contribute to protocol development, risk analysis, and operational efficiency improvements. Remote work is an option. The position offers the chance to positively impact lives within a team driven by innovation and high scientific integrity.

Requirements

• Requires a minimum of Undergraduate (Life Sciences preferred) degree, RN degree, or equivalent
• Experience in the pharmaceutical or medical device industry as a clinical research professional, including successful project leadership role and hands-on managerial experience running high quality clinical trials from inception to completion
• Excellent knowledge of international regulatory and ICH GCP guidelines
• Demonstrated success in coordinating external resources for clinical development and in working with pharmaceutical partners
• Demonstrated ability to manage large complex budgets
• Experience and understanding of the drug development process, clinical development planning and clinical trial execution
• Understanding of clinical aspects of therapeutic area along with willingness to develop in-depth expertise
• Prior experience using computer applications including spreadsheets, email, word-processing software & web-based systems (EDC, IVR/IWRS, CTMS)
• Ability to work well independently as well as a member of multiple, integrated teams
• Ability to contribute creative yet practical solutions to problems
• Ability to multi-task and manage several projects in parallel while paying attention to detail. A wide degree of creativity and latitude is expected
• Ability to be proactive in identifying issues and hurdles that may handicap the effective implementation of the trial and resolve the issues in a timely fashion
• Highly effective verbal and written communication skills with internal and external stakeholders
• Effectively collaborates with team members
• Ability to travel (including internationally) and work across cultures

Responsibilities

• Oversee and direct relevant clinical operations resources while also contributing to strategy, tactics, and driving execution of one or more global clinical programs, either at the regional or global level, depending on experience
• Influence, oversee and lead the planning, budgeting, and study management processes in global clinical studies, either at the regional or global level, depending on experience
• Responsible for UK, EU and Nordic region and potentially support studies at a global level, depending on study needs and individual experience
• Manage and lead to successfully manage external service providers including CRO(s), vendors and subcontractors, in addition to internal cross functional colleagues responsible for conducting global clinical trials to ensure project deliverables are executed on time and within budget
• Contribute to the development and operational design, planning, and strategy of clinical trial protocols and study and development plans
• Creates/supports scenario planning and risk benefit analyses to make recommendations to align with corporate strategies
• Contribute to models of performance excellence by identifying best practices, reviewing measurement systems and improving operational efficiency in department
• Review, assess and manage resource strategies with internal and external groups for global drug development programs, working strategically with suppliers/CROs
• Manage relationships with pharmaceutical partners and suppliers in clinical programs to optimize delivery
• Ensures efficient and effective communication and exchange of information across projects and reporting functions
• Participates in Clinical submission activities
• May serve as the clinical operations representative at regulatory agency meetings
• As needed, participates in due diligence activities for in-licensing opportunities
• Develop training plans, act as mentor and conduct performance reviews for all direct reports if applicable
• Supports the development and implementation of department level SOPs for clinical trials and related activities
• Interface with departments within and outside of Clinical Operations including Clinical Development, Safety, Finance, Clinical Supplies, Regulatory Affairs, Legal Affairs, and Business Development and any other departments as needed
• Represent the company at Investigator Meetings
• Other such duties as may be determined or assigned

Preferred Qualifications

• Advanced degree desirable
• Experience in direct line management preferred and hands-on experience in monitoring and managing high-functioning clinical trial project teams

Benefits

We are open to you working remotely