【主要な職務内容: Primary Responsibilities】
The purpose of the Diagnostics Development is to lead the development of diagnostic approaches and contributes to all drug development activity by using diagnostic tools. “Diagnostics tools” means not only PET but also other modalities and measurement tools
【PRIMARY RESPONSIBILITIES】
Management for manufacturing PET tracers in clinical trials
- Expertized technical support/training regarding PET tracers to the manufacturing sites.
- Management of manufacturing, certificating quality and recording processes to provide PET tracers
- Management of scheduling patients’ visit, manufacturing tracers, and training for staff at the sites.
- Coordinate and adjust the relationship with vendors (cost and time management)
- Provision of solutions regarding the matters in diagnostics for clinical trials
- Proposal of new tracers or devices to promote clinical trials.
- Consultation regarding diagnostics tools on the protocols for clinical trials
- Contact and negotiation with external organizations, and information feedback to LY for the matters in diagnostics regarding clinical development
- Build the strong relationships with external clients-TLs (Thought leader) and/or business partners.
- Other tasks regarding the specialties in diagnostics
- Support internal projects regarding diagnostics to promote internal tasks.
- Provide/share expertized information and trainings regarding diagnostics to promote internal tasks.
Business title: Associate/Manager/Sr. Manager-CD-CDCL
神経変性疾患(アルツハイマー病)の診断や治験遂行の中で重要な役割を担う診断薬「PET薬剤」の開発を行うグループ。
【QUALIFICATION REQUIREMENTS】
・Experience of drug development in pharmaceutical industry and/or working experience in the companies, institutes, departments expertized in nuclear medicine, radiopharmaceuticals.
・Language skill: Japanese ‐ Native level / English ‐ business level
・Excellent oral and written communication skills; able to communicate clearly and succinctly with team members and external organizations/partner companies
・Strong problem-solving skills; able to recognize problems before they become serious and take corrective action
・Excellent self-management and organizational skills are essential; able to manage workload and adjust personal priorities, as needed based on guidance from supervision
・Effective teamwork skills; able to adapt to diverse interpersonal styles.
・Flexibility to adjust quickly and effectively to frequent change and altered priorities
・Knowledge of drug development processes
・製薬/CROでの医薬品開発経験 or 医療機器/放射線医薬品業界での業務経験
・ビジネスレベルの英語
【Additional Preferences】
・Communication skill to build reliable relationship with external partners
・Higher degrees or certifications (e.g., master’s in health-related, scientific, engineering and Project Management) would be beneficial.
・Experience of working at companies/institutes/departments expertized in nuclear medicine.
・核医学関連のバックグラウンド
・ガスクロマト、液体クロマト等の分析機器の取り扱い知識/経験
多くの人が待ち望み、誰も作れなかった新薬を高度な技術で生産し、世界市場に届けます。
医師が安心して意見交換できる会員制サイト『MedPeer』。臨床の「集合知」が新しい価値を生み、ビジネス拡大中です。
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