Salario en Odonate Therapeutics

Requisitos

• bachelor’s Degree in Supply Chain or related discipline required
• bachelor's Degree in a Life Sciences discipline required
• minimum 10 years of experience in supply management and logistics within bio-pharmaceutical industry required
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• master's Degree, Bachelor's Degree in Nursing or RN a plus
• minimum 5 years of clinical trial experience required
• minimum 5 years of management experience required
• minimum 8 years of clinical trial experience required
• minimum 3 years of professional experience in the oncology therapeutic area required
• must be based in EU or United Kingdom
• bachelor’s degree in a life science required
• proficient in cGMP’s and pharmaceutical industry procedures and regulations
• bachelor’s degree in nursing discipline or RN a plus
• expert in supply and depot management globally
• detailed understanding of FDA, EMA, ICH and GCP guidelines and applicable local regulations
• minimum 3 years of direct site monitoring experience required; additional work experience, including experience at a biopharmaceutical company, preferred
• understanding of systems selection, design and management
• proven leadership abilities in a highly complex, dynamic and fast-paced environment
• minimum 1 year of work experience in the oncology therapeutic area is required
• outstanding written and verbal communication skills with the ability to effectively present to and engage with a wide range of audiences
• ability to inspire a collaborative team environment
• detailed understanding of all aspects of clinical site monitoring as well as understanding of overall global drug development required
• thorough understanding of FDA, EMA, ICH and GCP guidelines and applicable local regulations
• excellent critical thinking skills and ability to understand complex patient histories, medical terminology and oncology treatment landscapes
• strong organizational skills with the ability to manage projects, resources, timelines and budgets, in a fast-paced, entrepreneurial environment
• ability to interpret study level metrics data and proactively identify and mitigate risks through study lifecycle
• ability to effectively engage and influence internal and external leaders, solicit information, persuade others and shape outcomes
• madrid, Madrid provincia
• strong interpersonal skills and the ability to lead a team
• 08025 Barcelona, Barcelona provincia
• detailed understanding of all aspects of clinical protocol design and implementation, clinical site monitoring as well as overall global drug development required
• detail-oriented, organized and committed to quality and consistency
• results driven and capable of managing competing high-priority assignments
• problem-solving and decision-making skills
• proven track record of achieving deliverables within specified timelines
• demonstrated ability for analytical and systematic thinking
• excellent team-interaction skills and ability to work successfully in team settings
• ability to work in a dynamic environment with a high degree of flexibility