The Leidos Military & Veterans Health Solutions Group is hiring a counselor for our PACAF and Marines Adolescent Support and Counseling Services (ASACS) program. This program implements a community-based adolescent support and counseling program for the
ジョンソン•エンド•ジョンソンは,健康こそすべてだと考えています。ヘルスケアイノベ-ションにおける私たちの強みが,複雑な病を予防•治療•治癒し,治療をよりスマ-ト化した,低侵襲なものに進化させ,-人ひとりの患者さんに合ったソリュ-ションを提供することができる世界を築く力になります。 Innovative MedicineとMedTechにおける専門性を生かし,将来の飛躍的な進化に向けてヘルスケアソリュ-ションの幅広い領域でイノベ-ションを推し進め,人々の健康に大きなインパクトを与えていきます。https://www.jnj.com/ 職務概要 Position Summary: 複数のラインでの検査,包装工程における安全,品質,供給の全分野における要求事項の達 成に向けてチ-ムをリ-ドする。 Lead the team in the multiple inspection/packaging lines to achieve all requirements in safety, quality, and supply. 法規制の順守に関する責任 Regulatory Compliance Responsibilities: 全ての従業員はコンプライアンスの順守を最優先にしなくてはならない。 All employees must concern compliance as
Do you have a strong background in non-clinical activities? We are looking for a Non-Clinical Expert to join our team at Novo Nordisk. If you are ready to contribute to the development, submission, and approval of new
The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, youll be part
Our story Strada is a technology-enabled, people powered company committed to delivering world-class payroll, human capital management, and financial management solutions to organizations globally. With a team of more than 8,000 experts and over 30 years
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.
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.
* Responsible for preclinical of J-NDA * Contribute to the successful development of early projects and development pipelines from a toxicology and DMPK expert perspective 企業情報 * European multinational pharmaceutical and biotechnology company * Wide range of pipelines
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Manager, Clinical Operations ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to
We will use your ability to integrate/apply knowledge of global & Japanese regulations governing drug development to progressing Regenerons portfolio. This includes preclinical and clinical drug development programs, policies, and procedures. This is an exciting opportunity to demonstrate your knowledge
Job Description Summary -Lead the country Franchise Medical Team, develop the Franchise Medical Strategy and executes it through and operational Medical Plan. Coach and develop team members as well as represent Medical in country Franchise Leadership
At Regeneron, our medical affairs physicians and scientists are at the forefront of innovation, playing a crucial role in our global development organization. As a key liaison between Regeneron and the scientific and healthcare community, you will
Career CategoryRegulatory Job Description Group Purpose Japan Regulatory Affairs provides leadership, expertise, and execution for the regulatory strategy to obtain and maintain clinical trial and marketing licenses for Amgen molecules in Japan in alignment with local
Are you passionate about the world of clinical trials? Are you highly motivated by being able to make a difference in improving patients’ lives? The position of Clinical Research Manager provides you the opportunity to work
As a Senior Project Manager, you will partner with local and global teams to develop and execute comprehensive project plans that align local strategies with global objectives. This role is critical for maximizing the value of
The Solution Consultant, Global Trade role provides strategic prospective to customers with technical expertise, build quality relationships at senior levels with both IT and Business leaders and professionals, conduct thorough needs analysis for targeted demonstrations, uncover
As the Observational Research Program Manager, you will spearhead efforts to utilize real-world evidence to support drug development and regulatory decisions. Your role will focus on advancing research methodologies while enhancing organizational capabilities. 企業情報 A leading biotechnology company
Job Description SummaryContribute to the overall activities in drug development* toward obtaining the marketing authorization and maintenance activities of post marketing products in assigned TA area. * Drug development including development of drug, medical device, companion diagnostics and tissue-engineered medical products Job
About us BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline
