POSITION SUMMARY •Responsible for leading the MSL group activities. •Support for HCPs through timely dissemination of emerging scientific and medical information from amultitude of sources. •Analyze and identify key MSL insights, and provide to the DA
Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL. • Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and
Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL. • Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and
Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL. • Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and
Job Responsibilities: Sr. QA Specialist is responsible for all duties in Quality Department. Sr. QA Specialist reports to Sr. QA Manager. Principle Duties and Responsibilities : Sr. QA Specialist supports Quality Assurance related activities shown below:
A pharmaceutical sales role where you will leverage your understanding of the market and customer needs to promote the companys products, and build relationships with stakeholders. You will use your sales and market expertise to achieve the
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
* Takes accountability and serves as the first line of contact at the study level. 企業情報 * Top 3 Pharmaceutical Company * Rich pipeline with nice promotion space 職務内容 * Takes accountability and serves as the first
ROLE SUMMARY The Platform: The Chief Medical Affairs Office’s RWE Partnerships and Platforms organization is responsible for establishing global RWE data and scientific leadership through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic
Are you passionate about improving patient outcomes? Do you have experience in medical affairs and a desire to make a difference in the healthcare industry? We are looking for a Medical Advisor to join our dedicated
Are you an experienced medical professional and passionate about Medical Affairs? Are you a dynamic leader with a passion for driving MSL team? If so, we have an exciting opportunity for you to join our team
SUMMARY Responsible and accountable for Medical Affairs strategy of Urological cancer products C ollaborates with internal and external stakeholders including key opinion leaders to develop and implement the overall M edical Affairs strategy for product lifecycle
RESPONSIBILITIES/PRINCIPAL DUTIES: The Manager, IPN (Immunology, PAH and Neuroscience) Communication & Public Affairs, Janssen Japan is an important leadership role in our Japan Pharmaceutical Communication & Public Affairs (CPA) team responsible for our end-to-end communication strategy for
Responsibilities: * Lead the deployment of automation technologies to streamline the creation and updating of mandatory materials. * Conduct thorough evaluations of automation technologies tailored to pharmaceutical documentation needs. * Prioritize vendors with relevant experience and technical
企業概要 About us Publicis Groupe is not just a company you work for; it’s a platform for you to take your talent to the world. If you want to help change the world, ideas alone are
募集企業 武田テバファーマ株式会社 当社について 私たちは、世界中の数多くの人々がより健康的な生活を過ごすために、健康をより少ない負担で手にできるようにすることをミッションとして一体となって取り組んでいます。このミッションによって約60ヵ国に広がる多様な国籍や背景を持つ社員が結束しています。 当社で働くことは、世界をリードするジェネリック医薬品メーカーで仕事をすることであり、世界保健機関（WHO）の必須医薬品リストに収載されている医薬品を数多く製造していることを誇りにしています。今現在、世界中で少なくとも2億人の人々が、毎日、私たちの医薬品を服用しています。これは驚くべき数字ですが、弊社は常に、変化をもたらし続ける新しい方法と、変化をもたらすことのできる新しい人材を求めています。 採用の機会 今後、新薬およびジェネリック医薬品 (AG含む) に加えてバイオシミラーやスペシャリティ領域を手掛ける予定の当社で、あなたのファーマコビジランスのご経験に磨きをかけていきませんか？ 若手の活躍するワークライフバランスのよい職場にぜひあなたをお迎えしたいと思っています 会社での一日 市販薬ならびに治験薬の国内及び外国における有害事象情報を収集、評価、検討し、PMDAならびにGlobal へ報告する 市販薬ならびに治験薬の適正使用に関する安全性情報を医薬関係者等へ伝達する資料を作成する GVP省令ならびにGCP省令で求められている安全性定期報告等その他安全性業務に関する法規制の要求事項について、シニアメンバーのサポートを受けながら対応する GVP業務委託先製薬企業と連携の上、ファーマコビジランス業務が適切に行われるよう調整を行う GVP業務委託業者(CRO)の業務遂行状況を管理し、指導する Global PVならびに海外の規制情報の要求事項を理解し、シニアメンバーのサポートを受けながらファーマコビジランス業務を遂行する 変更の範囲： 当社業務全般への変更の可能性があります 職務経歴と資格 必須経験 新薬メーカーでの安全性関連業務経験者で3年以上の経験 英語スキル （読み書き必須。会話あれば尚可） あれば尚可 薬剤師 獣医師 看護師 よりやりがいのある選択を行う 雇用形態 正社員 勤務地 雇入れ直後：東京本社（東京都渋谷区恵比寿４－２０－３恵比寿ガーデンプレイスタワー18階） 受動喫煙対策
This pivotal role combines the excitement of crafting innovative clinical development strategies tailored to specific indications/products, ensuring their safety and efficacy for swift global registration, while also offering the opportunity to shape regulatory strategies and contribute
Are you a strategic leader with a commercial mindset? Are you interested in driving market access strategies for life-changing products and services? We are looking for a dedicated Local Market Access Senior Group Manager to join
企業概要 Syntegon Technology is a leading global process and packaging technology provider. Around 5,800 colleagues in more than 15 countries work for the Syntegon Group on intelligent and sustainable technologies for the pharmaceutical and food industries. At
* Responsible for managing PV projects for global pharmaceutical companies, including safety periodic report creation and literature screening, while collaborating with offshore teams. Great opportunity to broaden business skills through managing various PV tasks, team building. Client
