• drive Data Governance activities across Business Segments • work with Business Owners to ensure assignment of Data Stewards • produce plans for the governance of critical data assets and information • accountable for day-to-day Data Governance Operations oversight • facilitate data-decision making processes and discussion to address conflicting viewpoints • guide enterprise stewardship needs for training, information sourcing; provisioning; consumption; standardization; and reporting & analytics • ensure data adheres to all business and enterprise standards and frameworks • develop & drive data quality management as a core component • lead cross-functional committee and Enterprise Data Governance Leadership council • provide coaching and development opportunities to the team

• Provides strategic leadership for clinical pharmacy initiatives across all lines of business • Oversee formulary, criteria, and prior authorization activities to ensure timely, compliant, and high-quality service delivery • Accountable for monitoring drug utilization trends, guiding performance standards, and ensuring regulatory compliance to support affordability and member outcomes • Lead the strategic direction, development, and execution of drug management programs • Direct leadership staff responsible for formulary creation, criteria development and maintenance, prior authorization evaluations, and utilization management monitoring • Oversee development and maintenance of clinical pharmacy policies and ensure compliance with accreditation standards (e.g., URAC, NCQA, CMS) • Lead and develop a high-performing team, fostering a culture of accountability, engagement, and continuous improvement, and professional growth • Coordinate with pharmacy benefit strategy leaders and corporate stakeholders to deliver competitive and cost-effective clinical services • Lead audit preparation and compliance initiatives to ensure coverage review operations meet internal and external standards • Ensure clinical functions meet expectations for value and affordability, driving continuous improvement and market responsiveness

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Parabilis Medicines is seeking a Senior Director, Clinical Sciences to provide scientific and strategic leadership across our clinical development programs. This role is central to translating discovery and preclinical innovation into high-quality, data-driven clinical development strategies that advance our pipeline efficiently and responsibly. As Senior Director, Clinical Sciences, you will: - Lead and own clinical science strategy for one or more clinical programs across development stages - Drive scientific input into protocol design, endpoint selection, and clinical development plans - Serve as a core contributor to regulatory interactions, governance decisions, and program reviews - Influence portfolio strategy through integrated clinical and translational insights - Partner closely with Clinical Operations to ensure scientifically sound and feasible trial execution - Interpret and contextualize clinical, biomarker, and safety data to inform decision-making - Contribute to regulatory documents (INDs, IBs, briefing packages) and regulatory interactions - Support investigator meetings, advisory boards, and external scientific communications - Ensure consistency of scientific messaging across internal and external stakeholders - Mentor and guide junior clinical scientists as the organization grows - Leverage AI-enabled tools to enhance clinical insights, literature analysis, data interpretation, and operational efficiency Qualifications - PhD, PharmD, or equivalent advanced degree in life sciences, medicine, or a related field - 10+ years of experience in clinical development or clinical sciences within biotech or pharmaceutical settings - Direct experience supporting or leading clinical trials (Phase 1–3 preferred) - Proven track record of contributing to successful clinical programs and regulatory milestones - Deep understanding of clinical trial design, endpoints, and regulatory requirements - Experience working with clinical data systems, trial databases, and scientific literature platforms - Familiarity with biomarker and translational data integration - Strong scientific writing and data presentation skills - Experience in rare disease, oncology, immunology, or other complex therapeutic areas (as applicable to Parabilis’ pipeline) - Prior leadership or matrix-management experience - Experience interacting with regulatory agencies and external experts - Strong strategic thinking combined with hands-on execution - Comfort operating in a fast-paced, evolving biotech environment - Demonstrated use of AI tools in your current role and responsibilities is required. Advanced or innovated use of AI is a strong plus. Benefits - Base salary range: $265,000–$305,000 per year, depending on experience, qualifications, and internal practices - Annual target bonus - Equity - Comprehensive suite of competitive benefits designed to support employees’ overall well-being Core Values - Growth-Minded: We’re inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable. - In(ter)dependent: We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options. - Patient-focused: We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact. - All-In: We’re All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.

• Serve as the indication expert biostatistician and lead all statistical activities of a major indication (across assets) • Drive novel approaches and optimize the process across all stages of clinical development in the indication you are responsible for • Drive quantitative data strategy of the indication you are responsible for • Collaborate with stakeholders and lead delivery of all statistical deliverables • Oversee delivery of all statistical deliverables for the indication you are responsible for and contribute to HA submissions • Report to a franchise team leader, within the Biostatistics and Modeling organization • Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements • Guide the team of statisticians supporting the different assets