Senior Clinical Trial Leader Oncology

pThe Senior Clinical Trial Leader Oncology acts as the face of Alentis towards external vendors and partners, fostering strong and collaborative relationships, and manages and executes all aspects of clinical trial preparation and conduct, ensuring high-quality delivery and compliance throughout the study lifecycle. /p h3Tasks /h3 ul liAct as the primary Clinical Operations and/or Clinical Science lead and the face of Alentis towards external vendors, CROs, investigators, and study partners. /li liLead and oversee the preparation, execution, and delivery of complex global clinical trials, ensuring adherence to timelines, budget, quality standards, and regulatory requirements. /li liProvide strategic leadership and operational oversight for one or more clinical studies and support cross-study alignment across development programs. /li liContribute to and coordinate the development, review, and approval of study documents such as protocols, ICFs, study-specific guidelines, regulatory documents, monitoring plans, data management plans, statistical analysis plans, and clinical study reports, in accordance with internal SOPs and GCP requirements. /li liContribute to the preparation of regulatory submissions and responses to Health Authorities, ECs/IRBs, DSMBs, and other regulatory bodies. /li liContribute to the safety data monitoring and signal finding in collaboration with clinical development physicians. /li liOversee forecasting and planning of IMP, ancillary supplies, and study materials to ensure uninterrupted study conduct. /li liReview and approve feasibility assessments (RFI, RFP), contribute to vendor selection, contract negotiations, and vendor oversight strategies. /li liPlan, organize, and lead Investigator Meetings, vendor meetings, and study-specific training activities. /li liEnsure delivery of studies within planned timelines, quality expectations, and approved budgets. /li liOversee monitoring activities and review study performance metrics to ensure data integrity, protocol compliance, and patient safety. /li liProactively identify operational risks and study challenges, develop mitigation plans, and elevate critical issues to senior management as appropriate. /li liSupport and coordinate inspection readiness activities, audits, inspections, and CAPA management to ensure successful outcomes. /li liEnsure that study documentation is maintained, inspection-ready, and appropriately archived within the (e)TMF. /li liOversee database lock, study close-out, and study reporting activities to ensure timely completion of clinical milestones. /li liProvide strategic Clinical Science and/or Operations input into the Clinical Development Plan and broader program planning activities. /li liDrive continuous improvement initiatives and contribute to the development and implementation of clinical processes, standards, and SOPs. /li liMentor and provide guidance to Clinical Trial Leads, Clinical Trial Managers, and cross-functional study team members as appropriate. /li /ul h3Requirements /h3 ul liMaster's degree or equivalent university degree in Life Sciences, Healthcare, Pharmacy, or a related field. /li lib≥8 years of clinical study management experience, including early-phase clinical trials, preferably within biotechnology and global development environments. /b /li liDemonstrated expertise in global clinical trial leadership, clinical data signal detection, project management, and risk management. /li liExperience leading complex, multinational clinical studies and managing multiple stakeholders across countries, functions, and vendors. /li liStrong understanding of the oncology drug development process from First-in-Human through later-stage clinical development. /li liAdvanced knowledge of current clinical trial regulations and guidelines, including ICH-GCP. /li liProven experience in selecting, managing, and overseeing CROs and external service providers. /li liStrong understanding of clinical trial budgeting, forecasting, and resource planning. /li liDemonstrated leadership, influencing, and stakeholder management skills. /li liExcellent communication, presentation, and organizational skills. /li liFluent in English; additional languages are advantageous. /li liAbility and willingness to travel internationally. /li liProactive, solution-oriented, and capable of operating effectively in a fast-paced biotech environment with an entrepreneurial mindset. /li liFor the Basel workplace, candidates must hold a valid Swiss work permit or be EU citizens eligible to work in Switzerland. For the US workplace, candidates must hold valid US work authorization or be US citizens. /li /ul #J-18808-Ljbffr