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Senior Director, Clinical Excellence Leader
Alentis Therapeutics. Lead harmonization of cross-study fit-for-purpose practices across development programs to elevate the quality and productivity of deliverables .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in global clinical trial leadership, project management, and risk management within the biotechnology sector. Proven ability to foster collaboration and continuous improvement across cross-functional teams while ensuring adherence to regulatory requirements and quality standards.
Highest-signal resume keywords
Global Clinical Trial LeadershipClinical Data ReviewProject ManagementRisk ManagementOncology Drug Development
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical ScienceOperational ExperienceEarly-Phase Clinical DevelopmentSignal DetectionCross-Functional Team Leadership
Soft Skills
Excellent CommunicationStakeholder ManagementOrganizational SkillsCollaborationAccountability
Certifications & Qualifications
Master's Degree in Life SciencesSwiss Work Permit or EU Citizenship
Industry Keywords
BiotechnologyClinical DevelopmentRegulatory RequirementsQuality AssuranceCapability Building
About the role
Key responsibilities & impact- Lead harmonization of cross-study fit-for-purpose practices across development programs to elevate the quality and productivity of deliverables
- Drive the development, alignment, implementation, and continuous improvement of cross-functional clinical development processes and standards
- Serve as a role model and subject matter expert in planning, executing, and delivering complex global clinical trials
- Ensure adherence to timelines, budgets, quality expectations, and regulatory requirements
- Identify operational risks and implement proactive mitigation strategies to support program success
- Foster a culture of excellence, collaboration, accountability, and continuous improvement across clinical development teams
- Partner with Clinical Operations, Clinical Science, Clinical Development, Biometrics, Regulatory Affairs, Quality Assurance, and other internal partners to optimize study execution and decision-making
- Support capability building, knowledge sharing, and process scalability
Requirements
What you’ll need- Master's degree or equivalent university degree in Life Sciences, Healthcare, Pharmacy, or a related field
- Minimum of 15 years of clinical science and operational experience, including experience in early-phase clinical development
- Experience gained in both biotechnology companies and global drug development environments
- Demonstrated expertise in global clinical trial leadership, clinical data review and signal detection, project management, and risk management
- Strong understanding of the oncology drug development continuum from First-in-Human (FIH) through late-stage clinical development
- Proven ability to lead, influence, and align cross-functional teams in a dynamic environment
- Previous people leadership experience is advantageous
- Excellent communication, stakeholder management, and organizational skills
- Ability to thrive in a fast-paced, entrepreneurial, and rapidly evolving biotechnology environment
- Candidate needs to hold a Swiss work permit or be an EU citizen eligible to work in Switzerland
Benefits
Comp & perks- Indefinite contract (Unbefristeter Arbeitsvertrag)
- 3-month probation period
- 42 hours/week
- 25 days of annual leave
- Hybrid work arrangement with 3 days a week on-site