About the Role
This role is responsible for leading clinical operations in neuroscience, managing global trial execution, driving process improvements, and ensuring adherence to timelines, budgets, and regulatory requirements across all phases of development.
Responsibilities
- Lead the planning and execution of global clinical trials within the neuroscience therapeutic area.
- Oversee the development of clinical operations strategies aligned with program goals.
- Manage relationships with clinical research organizations and other third-party vendors.
- Ensure clinical trial timelines, budgets, and quality metrics are met.
- Collaborate with cross-functional teams including clinical science, regulatory, and data management.
- Serve as primary point of contact for clinical operations across internal stakeholders.
- Develop and implement risk mitigation plans for clinical study delivery.
- Oversee site selection, activation, and performance monitoring across regions.
- Ensure compliance with Good Clinical Practice and applicable regulations.
- Lead vendor selection and performance oversight, including CROs and central labs.
- Drive process improvements to enhance efficiency and data quality in trial conduct.
- Support the development of study protocols and essential trial documents.
- Monitor study progress and report key performance indicators to leadership.
- Ensure robust clinical trial monitoring strategies are in place and followed.
- Participate in global team meetings and contribute to program decision-making.
- Manage resource allocation and capacity planning for clinical operations team.
- Provide input into clinical development plans and regulatory submissions.
- Ensure patient safety and data integrity throughout trial lifecycle.
- Support inspection readiness and audit preparedness for clinical operations.
- Lead training initiatives for internal and external study team members.
- Foster strong collaboration between clinical operations and other departments.
- Evaluate new technologies and tools to optimize clinical trial execution.
- Contribute to the development of standard operating procedures.
- Ensure diversity and inclusion goals are considered in trial design and recruitment.
- Support corporate initiatives related to clinical development excellence.
Compensation
Competitive salary and comprehensive benefits package including equity and performance bonuses.
Work Arrangement
Hybrid work model with flexibility based on role and location.
Team
Part of the global clinical development team, reporting to senior leadership with cross-functional collaboration across research, regulatory, and data functions.
Why Join Us
We are advancing groundbreaking therapies targeting protein degradation to treat neurodegenerative diseases. Our science-driven culture values innovation, collaboration, and patient impact. You will work alongside experts in neuroscience and clinical development, contributing to transformative medicine from early to late-stage trials. We offer professional growth, inclusion, and the opportunity to shape emerging clinical programs.
Our Commitment to Diversity
We believe diverse perspectives drive better science and stronger teams. We actively foster an inclusive environment where all voices are valued, and differences are respected. Our hiring practices reflect a commitment to equity and representation across gender, race, background, and experience.
Available for qualified candidates requiring sponsorship.
