Site Engagement and Alliance Manager I/II
职位描述
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机会的企业,我们将考虑所有符合条件的求职者就业。不因残疾、性别或性取向、怀孕或产假状况、种族或民族或族裔出身、年龄、宗教或信仰、性别认同或变更、婚姻或伴侣关系、受保护的退伍军人身份(如果适用)及任何其他受法律保护的特征而产生歧视。】
企业简介
阿斯利康是全球领先制药公司,由前瑞典阿斯特拉公司和前英国捷利康公司于1999年合并而成。阿斯利康在6大治疗领域为患者提供富于创新,卓有成效的医药产品,包括消化、心血管、肿瘤、中枢神经、麻醉和呼吸等,其中许多产品居于世界领先地位。
阿斯利康总部位于英国伦敦,研发总部位于瑞典。产品销售覆盖全球100多个国家和地区。2005年公司销售收入为240亿美元。
阿斯利康拥有强大的研发能力,平均每个工作日的研发投入达到1400万美元 (2005年研发总投入为34亿美元)。我们在7个国家设有11个研发机构,共有11,900名员工从事与新药研发相关的工作。
阿斯利康拥有极具希望的早期开发产品组合,共有45个项目处于临床前研究阶段、17个项目处于一期临床研究阶段、13个项目处于二期临床研究阶段、6个项目处于三期临床研究阶段。
阿斯利康在全球19个国家有27个生产基地,共有14,000名员工致力于为客户提供安全、有效、高质量的产品。
阿斯利康在全球共有65,000名员工,从事医药产品和医疗服务的研发、生产和销售业务。
阿斯利康被列入道琼斯可持续发展指数(全球)以及显示企业良好社会责任度的富时社会责任指数(FTSE4Good Index)。
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职位发布日期: 2025-03-31