长沙招聘

Responsibilities:

Be responsible for planning, implementation and daily handlings of shipment orders to ensure clinical trial materials are well- supplied in accordance with the cGMP standards.

1. Perform all processes in accordance to established procedures and cGMP standards

2. Support the activities of planning, implementing, motivating, co-monitoring, and tracking study documents and tracking tools

3. Coordinate to ensure the shipment orders processing in a timely and accurate manner in accordance with cGMP standards

4. Confirmation of previously entered data and completion of data entry

5. Complete regular reports (as required by Management or client) pertaining to relevant work areas

6. Support PM to update contact listings, update checklist, generate and compile reports as requested.

7. Other job assigned by supervisor

Minimum Qualifications:

Education: college diploma above

Years of Experience: 1-2 yrs relevant working experience. Experience in freight operation, logistics management or international trade.

Knowledge: Logistics, international trade.

Competency: Good command of English; good command of MS office application; communication and coordination skills; customer-oriented.

Preferred Qualifications:

1. College diploma holder

2. Communication and coordination skills

3. Customer – oriented

PPC佳生集团（PPC Group）是一家成立于1997年的临床CRO公司。总部设立于上海，并分别在台北，徐州，北京，南京，首尔及东京设立了分部及分公司。
     自成立以来我们始终致力于为国内外制药企业及生物技术公司提供专业的临床研究服务及生物样本分析服务。至今，PPC佳生已经完成了超过3000项早期临床试验项目及超过500项II期至IV期临床试验项目，其中涉及24个主要研究领域。
     另外，PPC佳生的I期临床中心及生物分析实验室也分别通过了美国FDA,中国NMPA,台湾TFDA,日本PMDA,欧盟EMA及马来西亚NPRA等的核查。
     2012年，PPC佳生在台北（MacKay Memorial Hospital）建立了***家专属I期临床研究中心；2017年初与徐州医科大学合作共同建立了徐州医科大学附属医院I期临床研究中心；2018年，PPC佳生又分别与徐州市中心医院，湖北省鄂东医疗集团黄石市中心医院以及上海市浦东新区人民医院共同建立并开设了三家专属的I期临床研究中心。截至目前，PPC佳生已有5家自主运营的I期临床中心。