长沙招聘

职位描述：
Leads the development and implementation of medical coding in clinical data management systems.
Participates in management of individual case safety reports (SAEs, AEs of Special Interest, and Adverse Drug Reactions), AE/SAE reconciliation and data retrievals from the clinical and/or safety databases.
Provides support for endpoint adjudication committees.

1. Responsible for effective and efficient development of the coding conventions and coding dictionary license confirmation forms.
2. Manages quality control review of coded data.
3. Writes AE/SAE reconciliation plan.
4. Performs quality control of minimal data entry of safety data into WuXi CDS’s or sponsor's safety database.
5. Assures consistency of plans with client contract and identifies out of scope activities promptly and accurately.
6. Participates in internal and client meetings.
7. Reports project status to project/functional manager.
8. Adheres to financial and administrative processes, such as managing project budget and timelines, estimation of resource needs and projected hours.
9. Proposes solutions for procedural and technical issues.

Qualifications:
1. 2-3 years’ experience in medical coding using MedDRA and WHO Drug Dictionaries and/or
2. 2-3 years’ experience in entering SAE/ADR data into safety databases and/or
3. 2-3 years’ experience as a Clinical Data Coordinator
Basic knowledge in Pharmacovigilance 举报 分享

康德弘翼（WuXi Clinical），是药明康德（WuXi AppTec）的一家全资子公司。始终致力为全球客户提供全方位的临床研究服务，包括药品、生物制品、医疗器械、体外诊断试剂等医药产品。从I期临床研究到最终申报注册，通过严格的质量控制体系和专业团队的丰富经验，帮助创新性，突破性医药产品尽快上市和造福患者。

康德弘翼立足中国，面向世界，以上海总部为中心，辐射全球制药公司、生物技术公司以及医疗器械公司。目前，公司实行中美联合运营，人员规模达850人，覆盖中美两地，全国30多个主要城市，在上海、北京、广州、武汉、成都、长沙、西安、沈阳和美国奥斯汀、圣地亚哥10个城市均设有办公室。公司团队与各研究中心建立了良好的合作关系，始终保持着紧密的业务交流，保证了项目能高效、高质地完成。

随着业务能力的不断提升，我们已将业务范围成功扩展到美国、欧盟和亚太地区的部分国家。2018年7月，药明康德成功收购位于德克萨斯州的一家美国临床研究机构并实现中美联合运营，2019年5月，再一次收购了位于圣地亚哥的临床研究服务公司Pharmapace，这让WuXi Clinical的规模再一次得到扩大，进一步完善和增强了我们全球一体化研发服务平台的综合实力，帮助全球创新合作伙伴更好、更快地开发医药产品。