Location： Global Innovation Center Division： Sustainability & Communication Department Job level： Staff Report to： Group Manager Contract type： Full time Roles & Responsibilities グローバルイノベーションセンター発の研究開発に関連するPR戦略策定/実行を主要関連部門、社外パートナーと連携しプロジェクトをリードする。 PR戦略立案： R＆D発の技術やイノベーションを全てのステークホルダーに分かり易く伝達・見える化し、資生堂R&Dの話題性を高めるPR戦略を策定する。 自ら競合他社や社会環境、自社R&D戦略に関する情報を入手・分析し、GIC内外の関連部門や社外パートナーと積極的にコミュニケーションをとり、 ビジネス貢献や技術プレゼンス向上を目指す。 PR戦略実行： 策定した戦略の実現に向けて、技術情報を届ける目的やターゲットを常にクリアにしながら、最適なPRアクションやKPIを企画・検討し、その実行をリードする。 具体的には、イベント企画実行、技術リリース・ファクトブック・QA作成、取材対応実務、アセット制作・デジタルPR・SNS発信等。 Requirements ・広報・ブランドPR・IR・マーケティングのいずれかの分野で3年以上の経験 ・日本語ネイティブレベル ・英語TOEIC730点相当の英語力（主に英文リリースの校正） ＜その他歓迎要件・求める人物像＞ ・研究開発・技術・サステナビリティに関するPR・広報の経験 ・議論を構造化・可視化でき、討議における意思決定をリードできるファシリテーション力 ・コミュニケーション部門として、関連部署との連携・調整をマルチタスクで迅速に対応できる方
At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your
■ 職務内容 / Job Description Monitor is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in
■ 職務内容 / Job Description Lead Safety Information Management Group to manage pharmacovigilance activities incl. collecting, evaluating, and submitting safety information to relevant parties (e.g. PMDA, AZ global Patient Safety, licensing partners) and lead communication (incl.
Title: Medical Advisor / Medical Scientific Liaison FOP Company: IPSEN K.K. Job Description: As part of the Medical Affairs department, the MA/MSL is a hybrid, field-based scientific expert to external and internal stakeholders delivering non-promotional information
1. Specific department duties as set forth in the task list and department Training Checklists including but not limited to: a) Ensure timely processing of kits and requisitions b) Participate in the kit receipt process and
Join the team as a Finance Director! Shape financial strategy, impact patient care, and collaborate across departments. Make a difference in healthcare. Client Details Our client is a leading healthcare organization. With state-of-the-art facilities, a collaborative
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.
1. Regulatory requirement a. Breath analyzer testing requirements as per DGCA guidelines. This will involve the following. To carry out pre-flight / post-flight Aircrew and ground staff BA. Checking serviceability of BA instruments along with their calibration
Eligibility Criteria: 1. For any experience of 1 year (non-aviation in service industry or aviation industry) +12/ Diploma is mandatory 2. Graduation is mandatory for freshers and degree certificate is essential. 3. Candidates should not have
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
