Job Title: Remote Clinical Counselor This position is fully remote and candidates must be located in the OCOPAC region: Japan or Guam. All candidates must be flexible to work a shift within the hour range of OCONUS
1. Objectives Responsible for clinical development of the assigned project in Japan under the supervision of the Japan Development Leader (JDL), who assumes responsibility for development of all projects in Japan in the respective therapeutic/disease area (TA/DA).
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Basic Purpose of the Job Supports the complete clinical/pharmaceutical drug lifecycle process (research, development, market access, and market supply) by providing: Strategic planning and execution Data transformation Descriptive analytics Diagnostic analytics Predictive analytics Prescriptive analytics Work involves
Basic Purpose of the Job Key contact partner in cultivating the power of data by means of: Data collection/curation, data review, data delivery Data standardization Process definition, testing and training Translate scientific requirements into technical specifications.
General Information Job Advert Title: Clinical Site Manager Ⅲ（臨床開発モニター/ Site Monitor/ CRA） Location: Nihonbashi, Tokyo Division: Clinical Operations, Quantitative Sciences and China Development Employment Class: Permanent Description 【About Astellas】 Astellas is a global life sciences company committed to
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Japan Study Managerは、日本国内において治験の管理・監督を担い、CROや治験実施医療機関と連携しながら、治験参加者の安全と福祉、治験の品質を確保し、治験の計画通りの実施をリードします。グローバル・ローカル双方と連携し、課題解決や進捗管理も担当します。 JOB SUMMARY & RESPONSIBILITIES Responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and Pfizer
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on
About the Team / Department You will join a global Project Management team supporting Linguistic Validation (LV) and eCOA projects for clinical trials. The team works closely with internal stakeholders, clients, and external vendors to deliver high-quality,
Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people
Basic Purpose of the Job Supports the complete clinical/pharmaceutical drug lifecycle process (research, development, market access, and market supply) through: Strategic planning and execution Data transformation Descriptive analytics Diagnostic analytics Predictive analytics Prescriptive analytics Works with data
Basic Purpose of the Job Key contact partner in cultivating the power of data through: Data collection/curation, data review and data delivery Data standardization Process definition, testing and training Responsibilities include: Translating scientific requirements into technical
The Role We are seeking a qualified and experienced Rinsho-shinrishi 臨床心理士: Certified Clinical Psychologists and Konin-shinrishi 公認心理師: Certified Public Psychologists to join our growing team. The ideal candidate will have a strong background in delivering evidence-based treatments,
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
CRA II Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate
Job Description 医薬品開発プロジェクトにおけるプロジェクトマネジメントおよびアライアンスマネジメント業務 – プロジェクトマネジメントおよびアライアンスマネジメントのスキルや専門知識、一般的ビジネススキル、および疾患領域特異的な知識や経験を基に、部門横断的および戦略的視点からプロジェクトを推進する。 ・プロジェクトスコープの特定と開発戦略の立案を推進する。 ・開発戦略の実行状況やタイムライン等の進捗管理を行う。 ・リスクマネジメント、ステークホルダーマネジメントを遂行する。 ・ガバナンスとプロジェクトの接点となり、開発戦略の意思決定を推進する。 ・US本社プロジェクトマネージャーやチームメンバーと協働し、世界同時開発を推進する。 ・他社との協働にあたり、アライアンスマネジメントを遂行する ・特許等様々な観点から、製品の価値最大化に貢献する。 【必要なスキル・経験】 ・5年以上の製薬会社での勤務経験 ・3年以上のプロジェクトマネジメント（もしくはそれに相当する）経験 ・ビジネスレベルでの英語力 【尚可要件】 PMP (Project Management Professional) 資格 知的財産関連資格および実務経験 ※ Grade：P3 (Sr. Specialist)での募集ですが、ご経歴によりP2 (Specialist) やP4 (Associate Director)で採用する場合がございます。 Required Skills: Adaptability, Adaptability, Business
This is what you will do: Publication Lead collaborates with the Japan Medical Directors across-TAs as well as with the TA -specific Sci comms leads and medical directors. The successful Publication Lead will engage with internal
This is what you will do: Publication Lead collaborates with the Japan Medical Directors across-TAs as well as with the TA -specific Sci comms leads and medical directors. The successful Publication Lead will engage with internal