岗位描述
礼来对工作要求严格,因为患者没有等待的时间。我们以关怀之心探索创新之道,致力于让全世界人民过上更美好的生活。我们深知,每个决策、每个细节、每一天都至关重要。以位于印第安纳州印第安纳波利斯市的总部为中心,我们遍布全球的 50,000 多名员工积极应对复杂挑战,只为发现并提供改变生命的药物、深化人们对健康的认知与管理,并为我们所服务的社区提供支持。这是一项艰巨、紧迫且无私的工作,但值得我们付出。如果您心怀使命,并准备为真正关乎患者福祉的事业倾注全力,我们诚邀您加入我们。
Responsibility:
Responsible for assigned data management supporting tasks.
Ensure timelines and adequate quality of all deliverables for the assigned tasks.
Follow processes and adhere to Lilly and project specific standards (SOPs, GCP, and regulatory guidelines).
Establish and maintain effective communication within the study team.
Requirements
Education with scientific or health related field.
Knowledge in clinical trials.
Knowledge of medical terminology.
Proficient written and spoken English language skill
Skills in the SAS programming language preferred. (SAS编程语言)
Good communication skills.
Teamwork skills.
Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
Able to establish personal relationships with personnel from other line functions.
礼来致力于帮助残障人士主动就业,确保他们在竞聘职位时享有平等机会。如果您在提交简历来申请礼来的某个职位时需要便利,请填写便利申请表 (https://careers.lilly.com/us/en/workplace-accommodation),来获得进一步协助。请注意,这适用于在申请过程中要求提供便利的人员,任何其他通信将不予回复。
礼来不会因年龄、种族、肤色、宗教、性别、性取向、性别认同、性别表达、国籍、受保护的退伍军人身份、残疾或任何其他适用法律保障的状态而歧视任何申请人。
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