臨床開発本部は、日本国内外の臨床試験(治験)を通じて新しい医療機器の有効性と安全性を評価・検証し、厚生労働省(医薬品医療機器総合機構)へ承認申請を行い医療機器として製造販売承認を取得する業務を担います。 · ...

Clinical trial experience is required MD (Japanese medical license) holder limited to those with corporate experience (3-5 years or more) and development experience. · ...

Clinical trial experience is required. MD (Japanese medical license holder) with 3-5 years of company experience and development experience are limited. · ...

The Japan Sr Project Lead serves as the project lead for development pipelines with comprehensive responsibilities holding full independence. · ...

The GCDSE provides clinical and R&D expertise in various aspects of vaccine development. · ...

Deliver patient-centric studies from protocol design through to study report and archiving. Interface with Phase 1 Units, Clinical Research Organizations (CROs) and vendors to ensure assigned studies are delivered according to contract specifications. · Lead study specific decisi ...

Roles providing expertise on scientific topics regarding relevant disease areas and Company assets to ensure their safe and appropriate use by patients Acts as a field-based expert, building relationships with External Experts as trusted scientific partners. · ...

+ Job summary: For the assigned program/project(s) in the region: Assume overall responsibilities as a regional/country level Development Team leader in the matrix setting to ensure alignment across key stakeholders and promote team work. · + Qualifications: · • Bachelor's Degre ...

To manage the packaging, storage and the distribution of Investigational Medicinal Products (IMP's) and other clinical trial material in Japan. · ...

Manage local supply processes in Japan including roles and responsibilities of involved local and global functions as well as the SOP system that is aligned with global SOPs. Ensure best set-up, execution and closure of supply and distribution of Investigational Medicinal Product ...

As a Medical Writer, you will create high-quality regulatory-compliant clinical documents supporting product life cycle under supervision. You will work effectively with cross-functional teams and report progress of document preparation to the supervisor. · ...

The Pricing Strategist will be responsible to achieve UCB's Pricing & Access objectives for the pipeline portfolio (with focus on BKZ, rare diseases, Briviact and Staccato in mid-term). · Central to the role will be maintaining a clear view on priority opportunities to focus on,T ...

+Serve as a clinical and post-marketing medical safety expert in the country. · ++ · +(Preparation and writing of periodic safety reports) · + ...

The Medical Science Liaison is a field-facing role whose main objectives are to exhibit a high degree of scientific and clinical knowledge, · facilitate timely and appropriate scientific exchanges with external experts, · develop evidence generation plans to enhance the value of ...

The Cell Therapy Scheduling and Logistics Specialist I will be responsible for scheduling and monitoring patient treatment schedules for the manufacturing of Celgene's autologous cellular immunotherapy products. · ...

The Senior Marketing Manager will be responsible for leading a team of marketing professionals accountable for creating and operationalizing go-to-market strategies for existing and new market segments by incorporating customer needs, competitive dynamics, portfolio positioning, ...

Provides scientific expertise on relevant disease areas ensuring safe use of Company assets by patients. · ...

Provides Japanese Labelling & Artwork Regulatory expertise across a Therapeutic business unit. · ...