上海招聘

Job Summary:
? Assist in the development and implementation of solutions to DM service issues and concerns
regarding Medidata RAVE, Oracle Inform, CRF Design, and Data Capture or imaging
activities, including proactive prevention strategies.
? Develop and maintain programs for creation of datasets as per specifications.
? Create CRF annotations and Mapping specifications as per CDISC/Sponsor datasets.
? Develop programs to import external data and transform to SAS Dataset or Excel files for data
review and reconciliation.
? Maintain study databases for assigned projects.
? Perform programming for any regular or adhoc reports / listings as needed by the Study/Sponsor teams using available tools / SAS / Spotfire.

Responsibilities/Duties:
? Proactively learn to design and execute processes related to programming, setup, support of
clinical and/or safety databases like Medidata Rave or Oracle Inform or SAS programming.
? Perform the following duties with the guidance from Senior staff: Database design, EDC / SAS
edit programming, listings, ad-hoc/scheduled reports using SAS/Cognos/Business Objects – XI,
R and other tools for data cleaning and reporting.
? Complete assigned work utilizing EDC tools or SAS or other proprietary software according to
Covance SOPs, Work Instructions, and project specific guidelines in accordance with Good
Clinical Practices.
? Maintain knowledge and awareness of latest developments in CDISC standards and Statistical
programming.
? Create CRF annotations and mapping specifications as per Clients/CDISC standards.
? Develop and maintain SAS programs for creation of SAS datasets as per the specifications.
? Develop programs to import external data and transform to SAS Dataset or Excel files for data
review and reconciliation.
? Perform all work with knowledge of regulations pertaining to computerized systems to projects
to ensure compliance and interact with project team members in related discipline.
? Continuously learn and improve communication, technical, and problem-solving skills.
? Provide regular status update on the tasks assigned to Line Manager.
? Perform other duties as assigned by Managers and/or Senior Programming staff.

Experience:
? 3-5 years of relevant work experience to include data management and database support: EDC
systems programming or SAS programming.
? Good problem-solving skills and a proactive approach.
? Good oral and written communication skills.
? Good knowledge of clinical trial process and data management, biometrics, and systems
applications to support operations preferred.
? Ability to work in a team environment and under minimal supervision.
? Ability to prioritize work and Self-motivation.
? Appropriate time management skills and the ability to work to tight deadlines whilst maintain
the highest standards of quality work.
? A cooperative and team-oriented approach.

Education/Qualifications/Certifications and Licenses:
? University / college degree (life sciences, health sciences, information technology or related
subjects) or a certification in allied health professions from an appropriate accredited
institution.
? Fluent in English, both written and verbal.

LabCorp是全球***的生命科学公司，科文斯作为LabCorp旗下的药物研发部门，肩负着改善人类健康与生命的共同使命。科文斯的实验室和设施遍布全球，在世界范围内拥有超过26000名员工，卓越的研发能力和强大的人才资源奠定科文斯在医药研发行业的领先地位。截止到2020年，科文斯中国团队共参与了近100个获得上市许可的新药研发，积极支持超过50个免疫肿瘤药物的研发项目，是服务***面的药物研发公司。

欢迎加入科文斯中国团队，我们提供优厚的薪酬、完善的培训以及灵活的办公方式。也请关注“科文斯招聘”微信公众号，通过移动端迅速查询热招职位并投递申请，与我们并肩实现#CovancePotential。