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 shape the future of clinical development
Are you looking for your next “great mission” professionally? Do you feel like you have more to give, want to learn new skills and be part of a team with a rewarding mission supporting our Active-Duty
Do you enjoy negotiating and settling sales contracts for a global business? Do you have excellent organizational, analytical and contract drafting abilities? About our Team Elsevier Health applies innovation, facilitates insights, and helps drive more informed
Job Description A leadership role responsible for providing direction and management of the Strategy, Evidence Generation and Confidence activity in Hematology area of expertise. Proactively demonstrate the AZ Values. • Lead medical strategy creation in accordance
Job Description Summary The Study Leader is the leader of the cross-functional clinical trial team (CTT), guides planning andmanagement of the assigned clinical study/studies end-to-end to achieve Global Program Team(GPT), Global Clinical Team (GOT) and GCO objectives. Accountable for
Job Description Summary 割り当てられた治療領域と地域における医療専門家エンゲージメントおよび教育戦略を実施し、Reputation の向上に寄与する Job Description 上長の指示と同意のもと、割り当てられた治療領域と地域における医療専門家エンゲージメント計画を策定します。 Medica業務/エlクセレンスグループのBBOおよび戦略との整合性を確保するために、治療領域における医療専門家エンゲージメント計画を策定します。 現場で得られた医学的知見と医学的/科学的知見が地域におけるエンゲージメント計画に反映され、主要な問題が地域の同僚と適宜対処されるようにします。 該当する品質モジュールおよびその他の手順文書（SOPなど）を遵守しながら、自発的な臨床試験を設定、実施、追跡します。 医療専門家エンゲージメント計画に沿って MSL 活動の実施を推進し、重点バイオシミラー製品の認知度を高め、科学情報を提供します。 科学講演や対面ミーティングを通じて、医療コミュニティの専門家に科学的なメッセージを伝えます。 全国の医療専門家や医療コミュニティの専門家との強力なネットワークを構築します。 上長の指示と監督の下、結果を追跡してコンプライアンス チームに報告するなど、対象治療領域での助成金活動を運営します。 MRなどの他の部門と機能横断的に連携します。 科学的観点から現場の商業活動をサポートします（顧客の要求に応じて科学的情報を提供します） MR に対して製品（特に新発売製品）と疾患に関する科学的トレーニングをサポートします 割り当てられた治療領域におけるすべての活動とやり取りが、地域、世界、国内の法律、規制、ガイドライン、行動規範、会社のポリシー、およびベストプラクティスの受け入れられた基準に十分配慮して行われるようにします。 上長の指示の元に医療監査を準備します。 ベンダーが活動に関与する間ずっと資格を満たしていることを確認します。 影響を受けるすべての研究でコンプライアンスを遵守した安全性報告を確実に行うために、地域の医薬品安全性監視チームと提携します。 • Prior pharmaceutical industry experience within a medical function •
Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Job Title CT Clinical Scientist Job Description Job title: CT Clinical Scientist Key Areas of Responsibility 1.Identify and connect new customer needs, solutions and technologies to initiate new methods (or disruptive enabling technologies) of diagnosis, treatment and/or care
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.
MAIN REPONSIBILITIES / DUTIES JOB POSITION PURPOSE The MAS role family comprises a variety of medical scientific specialties, such as office Medical (oMAS) and field Medical scientist (fMAS). Be the Pfizer Japan medical scientific point of
Job Description Summary -Responsible for all statistical programming/data review reporting and analytics development aspects of assigned studies or project-level activities. Acts as a key contributor in ensuring that drug-development plans are executed efficiently with timely and
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Job Description: Key responsibilities: Liaises and supports development of KEEs Provides high quality medical and scientific support/communications to internal and external customers (e.g. advisory board meetings, training courses/workshops together with KEEs, support of speakers with presentations
Job Summary: Incumbent performs routine laboratory procedures in accordance with established Covance CLS quality principles, as well as trains new employees on the same. Incumbent is responsible for validating and maintaining new assays. Incumbent offers strong
JOB DESCRIPTION: Primary Function Abbott Medical Japan is seeking a dedicated and ambitious Clinical Study Specialist (CRA) to join our team. This mid-level position in Clinical Research is ideal for those aspiring to start or advance their career in
Cochlear is the global market leader in implant hearing solutions. Cochlears mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear
