🕒 26 days ago
Leads commercial data strategy, patient-level claims analytics, performance reporting, and advanced analytics, translating complex pharmaceutical data into insights and recommendations for commercial leadership.
Replimune jobs
Biotechnology company developing oncolytic cancer immunotherapies.
🏢 Biotechnology🎯 Oncolytic Immunotherapy
9 open roles at Replimune
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📅 Sep 30
Leads Medical Affairs scientific communications, shaping publication plans and ensuring study data, abstracts, and congress materials are accurate, timely, compliant, and compelling throughout the product lifecycle.
📅 Sep 25
Leads Commercial CRM operations and technology strategy, overseeing Salesforce, Veeva, Oracle, marketing platforms, integrations, and projects to strengthen customer engagement and support commercial teams.
📅 Sep 16
Leads clinical and scientific execution of oncology development programs, partnering across functions and with external collaborators to deliver compliant studies, analyze and present data, and support clinical development capabilities.
📅 Sep 11
Leads IT operations, infrastructure, and cybersecurity strategy, ensuring secure and reliable technology while managing risk, regulatory compliance, incident response, and business continuity across the organization.
📅 Sep 10
Leads and develops a regional Medical Science Liaison team, aligning field medical strategy with clinical and business objectives while ensuring scientific exchange, team performance, and regulatory compliance.
📅 Sep 8
Leads HR support for the UK site, advising senior leaders and employees on employee relations, performance, talent, and development while implementing people programs that support engagement and business growth.
📅 Aug 26
Leads early clinical development strategy and execution for oncology studies, guiding cross-functional teams from study design through analysis and reporting while mentoring clinical scientists and ensuring compliant delivery.
📅 Aug 6
Leads medical safety review and pharmacovigilance for assigned products across development and post-approval, including safety signal detection, benefit-risk assessments, regulatory documents, and cross-functional clinical team support.
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