募集要項
業務内容 |
Efficiently manage and successfully execute all aspects of global project start-up; Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Review pertinent regulations to develop proactive solutions to start-up issues and challenges; Present during bid defenses, general capabilities meetings, and audits. |
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雇用形態 | 正社員 |
応募資格 |
Bachelor’s degree or Master's/PhD degree within Life Sciences and more than 5 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience; Strong oral and written communication skills. Knowledge of pharmaceutical industry, International Conference on Harmonization guidelines, and FDA or applicable local regulations. Possess thorough understanding of regulatory submissions activities; Demonstrated ability to organize, instruct and supervise a team in the completion of multiple tasks/projects; Bilingual Japanese and English. Travel: Minimal |
英語力 | ビジネスレベル |
年収 | 780万 〜 1300万円 |
給与詳細 |
※経験・能力を考慮し、決定いたします。 基本給 年俸780万円~1300万円 *残業手当は残業時間に応じて別途支給 賞与実績:決算月に業績賞与あり 昇給:年1回 試用期間:6ヶ月 ※年俸制(年俸の1/12を毎月支給) |
勤務地 | 東京都 |
備考 |
企業情報
匿名
関連する求人
ACCOUNTABILITIES This position will report to the Head of Global CSR and is responsible for the project management of Global CSR Program and supporting the effective execution and tracking of day-to-day duties of its ongoing projects. Responsibilities include: Lead and manage Global CSR Program project planning, work plan development and monitoring, and reporting to ensure effective communications between program partners, the Global CSR team, and involved internal stakeholders. Coordinate routine reporting and monitoring of Global CSR Program partners, track progress and reporting on results (including outcome data), manage payment process and donation usage reviews, help identify and mitigate risks, and help resolve conflicts and issues. Ensure that a result framework for managing results is in place and regularly tracked for each new Global CSR Program project by closely working with Global CSR Program partners. This includes how the project contributes to sustainable impact, by defining outcome and output indicators and establishing baselines at onset and tracking progress towards targets. Contribute to further development of a result framework towards tracking and demonstrating by data the effectiveness and impact of our Global CSR Program Support the day-to-day management of Global CSR’s Digital CSR Donation Management System, an online portal used to receive proposals and coordinate reporting and monitoring of ongoing projects. Develop contents to demonstrate Global CSR Program partners’ impact using data, and collaborate closely with corporate communications teams to help develop regular and ad hoc project communications for internal and external audiences. Lead coordination of employee participation programs, online and onsite, to create learning and engagement opportunities for employees and support other employee engagement activities as part of the team. Support to Global CSR Program Request for Proposal (RFP) process, including serving as a proposal reviewer, with particular attention on evaluating applicant and shortlisted proposal budgets, and supporting the proposal budget and narrative clarification process, due diligence process, and donation agreement completion and awarding process with internal partners and awardees (as needed). Contribute to the design and drafting of research findings, publications, project updates, tool kits, guidance documents, presentations, and reports, as needed. Assist in the development of project communications for leadership. Support the Head of Global CSR to pursue opportunities for collaboration with other internal teams, helping to build a cross-cutting approach to global health work. Support the Global CSR team with additional tasks as needed. We are seeking a highly motivated, results-oriented individual with strong problem solving and analytical skills to support the Global CSR Program. This role entails working with an entrepreneurial, self-motivated mind-set. The candidate must be able to function independently, be flexible, and have strong commitment to excellence. This will involve attending calls and meetings with leadership, tracking action items and requests, and developing technical materials as needed for meetings and presentations, partnering with others internally and externally to resource various activities and ensuring appropriate follow up. We strive for a strong team environment, working in tandem with internal stakeholders within the enterprise, from finance and legal to corporate communications teams to execute our Global CSR Program. The Manager is a critical member of Global CSR’s lean, agile and dynamic team. A successful candidate will have a background/ interest in global health and philanthropy, be proactive and detail oriented with exceptional organizational, problem-solving, decision-making, analytical and communication skills. This role will rely on strong skills in building collaborations, partnering with broad stakeholder groups, working across global projects and teams, result management, clear communication (verbal and written), and strong time and people management. This role will also require using and embracing of data and technology. A successful candidate will be required to develop strong relationships with a variety of stakeholders, internal and external partners, and effective interactions with senior audiences. DIMENSIONS AND ASPECTS Technical/Functional (Line) Expertise We seek experienced professionals with a Bachelor’s degree and at least 5+ years of experience, preferably leading projects with expanding scopes of responsibility. Relevant work experience in roles focused on developing, implementing, and managing projects/programs. Broad understanding of global health/development issues and some global health/development experience is preferable. Experience in philanthropic grant management is a plus. Leadership Capable of influencing without ultimate decision-making authority, and gaining buy-in from various stakeholders to ensure successful implementation of programs. Able to understand all the shifting components of a project and what each entails while keeping the big picture front and center Demonstrated strength in structured problem solving, with the ability to easily identify and communicate frameworks to facilitate decision-making. Ability to work in a self-guided manner, and manage multiple priorities with demanding timelines. Ability to question and challenge colleagues including managers and partners in constructive manner. Accustomed to highly unstructured and ambiguous situations; ability to proactively resolve. Interaction Interacts with ease and appropriate discretion with key internal & external stakeholders (members and senior leaders in Global Corporate Affaurs, in other Business Units / Functions and senior representatives of non-government organizations, etc.) Innovation Demonstrated ability to think creatively to ensure successful management of results and completion of programs/ projects. Demonstrated ability to translate strategic and technical content from conversations into high-quality presentations and written communications in the framing and voice of a principal. Ability to think creatively to help organize information, manage workflow, and improve systems and processes. Ability to embrace data and technology Complexity An ability to execute efficiently across a wide variety of tasks and projects simultaneously. Excellent organizational, facilitation, oral, and written communication skills. Ability to work effectively and with sensitivity across barriers such as language, culture and distance. Excellent listening skills and compassion.
- 900万〜1300万
- 東京都
- 医薬品メーカー(先発医薬品)
募集中
CRAの直属の上司として、CRAのピープルマネジメント及び、医薬品の臨床開発において以下の重要な役割を担って頂きます: ■CRAを期待されるレベルに到達させるため、適応となるSOP、規制要件及びガイドラインの教育を行い、プロジェクトの品質を向上させる。 ■医療機関への同行及びモニタリング報告書のレビューにより、CRAのパフォーマンス評価並びに指導を行う。 ■CRAの実施医療機関に対する業務計画及び実行状況について、決められたタイムライン通りに実施出来ていることを監督する。 ■医療機関で発生した重要な問題の解決、是正措置及び予防措置の構築をサポートする。 ■CRAの目標設定及び中長期的なキャリア開発をサポートする。 ■状況報告のため、海外及び日本の治験依頼者との定期的なテレカンファレンス実施する。 【特徴】 取引先:大手外資系製薬メーカー 領域:オンコロジー領域、再生医療など最先端分野 実施試験:全てグローバル試験 監督するCRA数:最大12名
- 700万〜900万
- 東京都
- CRO
募集中
【職務内容】 ・事業計画に基づく臨床開発戦略の立案 ・GCP SOP や関連書類の管理、教育 ・リソースと予算の最適化 ・営業部門の予算管理ならびに案件獲得に向けた営業戦略の立案 ・将来的に新規事業の立ち上げやM&Aの促進など会社経営に関わる業務もお任せ致します。
- 900万〜1200万
- 東京都
- CRO
募集中
Line management of Clinical Research Associates (CRAs); Recruitment, initial and continued training and development of CRAs; Oversight and Management of CRAs to ensure CRAs are meeting expectations of core monitoring responsibilities; Tracking and management of CRA resourcing/allocation of assignment; and Manage turnover and retention of CRAs to meet company objectives
- 780万〜1300万
- 大阪府
- CRO
募集中