体外診断薬・医療機器の申請業務を担う · 国内薬事業務における申請業務・業態管理・当局との折衝や関連団体の窓口となるスペシャリストを募集します。 · 徐々に専門を広げ、富士レビオ全般の薬事申請にも関わって頂き、幅広い経験を積むことも可能です。 · ...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access equity all. · ...

We are seeking a highly motivated Regulatory Affairs Manager to lead regulatory strategies and ensure compliance for pharmaceutical and medical device products. This role plays a critical part in supporting product launches, ...

Are you ready to accelerate your potential and make a real difference within life sciences, · diagnostics and biotechnology? · ...

This Is What You Will Do · 担当地区における医療関係者とAlexionの主要窓口として、疾患及び製品の認知度を向上させ、患者様の為に診療環境の整備に努める。 · 担当地区(テリトリー)の状況分析に基づいた効果的なテリトリー戦略立案、戦術実行により設定された営業目標を達成する。 · 希少疾患における市場原理を十分理解し、優先順位の高い施設・医療関係者について具体的な攻略プランを策定、プランに基づくアクションを実行し、随時見直しを行う。 · ...

A Pharmaceutical Information Specialist is needed to provide high-quality services for stakeholders in the neuroscience therapeutic area. The successful candidate will be responsible for market analysis, sales growth strategies, resource utilization, customer engagement, · and co ...

Design analyze and interpret clinical trials/post marketing surveillance (PMS) in compliance with relevant regulatory requirements company standards and best practices Provide scientifically rigorous statistical expertise and contributions by working effectively within the clinic ...

+ 10 years' practical experience with CMC-related roles preferred (CMC regulatory affairs, Analytical/Quality testing, or Manufacturing) in Pharma Industry Advanced degree in medical, pharmaceutical or life-science etc Hard skills/ Expertise: Idealy + 10 years' practical experien ...

+ Job summary: At Johnson & Johnson we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented treated and cured. · + Qualifications:At least 5 years of pharmaceutical business experience with medical d ...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takadas Privacy Notice and Terms of Use. · ...

Design clinical trials/post marketing surveillance in compliance with regulatory requirements and company standards. · ...

We believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, · `Plan, prepare and execute necessary regulatory actions to support business objectives. · `}`Company's business strategy ...

+ At Roche you can show up as yourself , embraced for the unique qualities you bring. Our culture encourages personal expression , open dialogue , and genuine connections , where you are valued , accepted and respected for who you are · This is how we aim to prevent, stop and cu ...

This Is What You Will Do · Taking charge of the regional area and being the primary contact for medical professionals and Alexion, you will work to improve awareness of the disease and product among them, · and strive to establish good relationships with medical professionals by ...

Clinical Research Specialist role involves leading clinical trials planning and execution in collaboration with various departments. The specialist will be responsible for creating or reviewing related documents such as SOPs and managing trial milestones. · ...

At Johnson & Johnson, · We believe health is everything. · Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,treated,and cured, · where treatments are smarter and less invasive, · and solutions are personal. · ...

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? · ...

This Is What You Will Do担当地区における医療関係者とAlexionの主要窓口として、疾患及び製品の認知度を向上させ、患者様の為に診療環境の整備に努める。 · ...

We're looking for a Principal Specialist to join our QARA team in Tokyo. As a General Marketing Supervisor under the PMD Act, you'll ensure compliance with all applicable QMS and GVP requirements. · ...

This position requires the successful candidate to support the activities in RADDS Japan which includes contributing to the scoping, integrated proposal compilation, and delivery oversight of multi-disciplinary biopharmaceutical development advisory/clinical trial enablement proj ...

MR is required to contribute strong sales skills at the field level to support GSK Japan's growth strategy. · Detailed information provision activities based on business strategies and activity plans in assigned facilities. · Execution of new liver disease treatment drug launch a ...