The normal use of 1, the group responsible for the internal UFIDA NC system, and solve the problems in the use of;

2, responsible for the maintenance of ERP basic data and data correctness verification; collection and collation of the various departments to use the needs, to help find solutions and put into practice;

3, responsible for the preparation and carding of ERP business process; the new function of the test and the preparation of the test report;

4, the preparation of ERP system operating manuals, training documents, operating specifications and other project documents, to help organize the implementation of ERP internal training;

5, bear the ERP system data backup and system reliability and security work, for the system data security and business continuity is responsible for;

6, coordinating the implementation of software vendors and the group and the group and the group of business users to promote business processes to optimize and meet business needs.

1, familiar with server management, with the SERVER SQL database or ORACLE database basic operation and maintenance capability;

2, skilled in UFIDA NC management software, a petrochemical industry experience is preferred;

3, received ERP project management, system management training, more than 3 years of ERP project implementation management or development management experience;

4, familiar with the mainstream programming language, has a certain ability to develop;

5, there is a strong organization, coordination, planning and management capabilities, there is a need to analyze the ability to change the business needs of the Department of information language and the ERP system to achieve, there is a relatively deep foundation of the document;

5, computer, information management related major, bachelor degree above 6 years of experience, of which at least 3 years of experience in the implementation of ERP project management or development management.

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The organization and management of clinical trials, 1 research projects including: CRO screening of clinical research, and docking with the CRO mechanism, quality control and management for clinical research projects, supervise the completion of clinical trials according to the quality on time, launch and implementation and the end of work;

2, to assist in project research: responsible for the introduction, cooperation or independent option project clinical research data or data retrieval and evaluation, to provide support for the project;

3, assist in product registration: write, review the project and clinical research related to the application of information (including domestic and foreign registration);

4, the establishment and maintenance of clinical expert resources, as well as the company's internal medicine solutions and training related issues;

5, the completion of other tasks assigned by the leadership.

1, clinical medicine, pharmacology and other related professional bachelor degree or above, master degree is preferred;

2, 5 years or above in pharmaceutical or CRO clinical trials and management experience, the ability of clinical trials research projects with independent organization and management, clinical trials have innovative drug I-III (especially the international multi center clinical trial) is preferred;

3, familiar with the whole process of clinical trials and GCP specification, familiar with the development status of domestic and international clinical research and registration requirements;

4, English level six or above, be able to read and translate English documents, fluent oral English is preferred;

5, with strong organizational, communication and coordination and control ability, clear thinking, strong expression ability, and can adapt to travel.

Resume delivery mailbox HAIKEGROUP@163.com