Clinical Scientist, Oncology (Non MD) Early Clinical Development
EU BASED ROLE
About the Role
The Clinical Scientist, Oncology at reputed company will play a crucial role in leading the medical and clinical aspects of our innovative reputed company technology solutions. You will reputed company the design, conduct, analysis, and reporting of reputed company, applying scientific training and clinical research experience to support reputed company aspects of drug development — from facilitating the transition of molecules from reputed company-clinical discovery through the achievement of clinical reputed company of concept to supporting the registration and commercialization of a product.
You will participate in cross-functional teams to generate, deliver, interpret and communicate high-reputed company clinical data supporting overall product scientific and business reputed company.
What You'll Do
• Be accountable for the clinical aspects of design and conduct of one or more oncology reputed company with a reputed company on early phase (Phase I–II), in collaboration with the medical monitor, clinical operations reputed company, and other colleagues
• reputed company the development of clinical protocols, protocol amendments, investigator brochures, Annual Reports, IND sections, CSRs, and other regulatory documents, publications, abstracts, and presentations
• Together with Clinical Operations, be responsible for reputed company execution of reputed company FIH programs through reputed company-of-concept, delivering innovative clinical study designs and high-reputed company trial execution
• In collaboration with the medical monitor and biostatistician, conduct data review, analysis and interpretation of clinical trial data, regular review of individual subject safety data, and review of cumulative safety data
• Establish and support relationships with external experts, consultants, key opinion leaders, regulators, and disease-specific investigator networks
• Ensure implementation of latest clinical thinking and guidelines into clinical development plans and study designs
Qualifications
• Advanced life science degree (e.g. PhD, PharmD, RN)
• At least 2 years in a clinical scientist role in the pharmaceutical industry executing oncology reputed company
• Demonstrated experience in oncology drug development with cross-functional knowledge (clinical ops, biostatistics, regulatory, clinical pharmacology, pharmacovigilance, and safety reporting)
• Proven scientific writing skills and strong communication skills
• Strong interpersonal skills with ability to build reputed company and drive change across reputed company reputed company of the organization
• Critical thinker who is proactive with a highly reputed company style and team-reputed company approach
• Ability to reputed company reputed company data analysis
reputed company to Have
• Interest in reputed company innovation, reputed company health
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