Site Engagement and Alliance Manager I/II
職位描述
Job DescriptionThe Site Engagement and Alliance Manager I (SEAL Manager I) is the focal point of contact on strategic partnership collaborations between AZ R&D internal partners and key regional institutions/sites. It will coordinate with other roles and functions that will interface with key sites, thereby, streamlining AZ-site communication and ensuring productive site-level activities.The SEAL Manager I proactively collaborates with key sites to facilitate study start up and execution through local intelligence, process alignment and systemized workflow.Typical AccountabilitiesEstablish and coordinate strategic partnership collaborations with key sites e.g. building research capabilities such as translational research and process digitalisation, sharing of therapeutic expertise, R&D Forums/workshops.Set up and build new key sites with the site management team. Ensure coordination of clinical studies from site selection through site close out.Maintain regular contact with key site stakeholders and establish point of contact for institutional communication e.g. Bi-Annual key site leadership review meeting, site visits and remote updates.Facilitate the trial delivery in hospital level through the alignment of study start-up process and systemized workflow, such as key site Master Clinical Service Agreement template. Support issue handling to ensure the quality and speed of ongoing and new clinical trials in key sites.Participate in initiatives/activities as agreed with Line Manager (Head of DevOps/ Head of SEAL).Actively share applicable information that may be relevant to other functions such as key site intelligence and industry development trends e.g. early stage development, technology integration, key site capability and resource, site process and recruitment/quality metrics.Ensure compliance with AstraZeneca’s Code of Conduct and company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).Contribute to process improvements, knowledge transfer and best practice sharing.Education, Qualifications, Skills and ExperienceEssentialBachelor degree in life science or related discipline.At least 6 year working experience in pharmaceutical company, with basic knowledge in clinical research, preferred in multinational pharmaceutical companies or multinational CROs is preferred.Have proven track record on external stakeholders engagement.Fluent in both oral and written English.Excellent project management skills.Adapt to change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.Good analytical and problems solving skills.Excellent negotiation skills.Good ability to learn and to adapt to work with IT systemsExcellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP.Good knowledge of relevant local regulations.DesirableClinical trial operational experience is plus.Ability to work in an environment of remote collaborators.Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.Good cultural awareness.Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.Ability to manage crisis and complexity.Good medical knowledge in relevant AZ Therapeutic Areas.【AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.阿斯利康是一家提供平等機會的企業,我們將考慮所有符合條件的求職者就業。不因殘疾、性別或性取向、懷孕或產假狀況、種族或民族或族裔出身、年齡、宗教或信仰、性別認同或變更、婚姻或伴侶關系、受保護的退伍軍人身份(如果適用)及任何其他受法律保護的特征而產生歧視。】
企業簡介
阿斯利康是全球領先制藥公司,由前瑞典阿斯特拉公司和前英國捷利康公司于1999年合并而成。阿斯利康在6大治療領域為患者提供富于創新,卓有成效的醫藥產品,包括消化、心血管、腫瘤、中樞神經、麻醉和呼吸等,其中許多產品居于世界領先地位。
阿斯利康總部位于英國倫敦,研發總部位于瑞典。產品銷售覆蓋全球100多個國家和地區。2005年公司銷售收入為240億美元。
阿斯利康擁有強大的研發能力,平均每個工作日的研發投入達到1400萬美元 (2005年研發總投入為34億美元)。我們在7個國家設有11個研發機構,共有11,900名員工從事與新藥研發相關的工作。
阿斯利康擁有極具希望的早期開發產品組合,共有45個項目處于臨床前研究階段、17個項目處于一期臨床研究階段、13個項目處于二期臨床研究階段、6個項目處于三期臨床研究階段。
阿斯利康在全球19個國家有27個生產基地,共有14,000名員工致力于為客戶提供安全、有效、高質量的產品。
阿斯利康在全球共有65,000名員工,從事醫藥產品和醫療服務的研發、生產和銷售業務。
阿斯利康被列入道瓊斯可持續發展指數(全球)以及顯示企業良好社會責任度的富時社會責任指數(FTSE4Good Index)。
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職位發布日期: 2025-03-31