個案編號：

R45275E14

工作地區：

臺北市

工作類型：

全職

產業類別：

生物製藥藥品

職務類別：

生物醫藥科技

職務內容：

1. To be responsible for clinical trial submission, including preparation, application, follow-up the status until obtaining the approval.
2. Contact site to collect study and IRB required document.
3. Setup submission strategy and execute to meet the timeline.
4. Review, prepare clinical contract/budget in accordance with institutional requirements
5. To provide the recommendation about clinical contract/budget requirements and process, and resolution of comments and issues
6. On-site to discuss the budget with the investigator, and negotiate site contract and budget with site
7. Coordinate contract execution and timeline management to target site activation
8. Provide local expertise to RSUM and Project team during initial and on-going project timelines planning
9. Perform quality control of documents provided by sites

薪 資：

NTD / 面議 （經常性薪資達4萬元或以上）

福 利：

依法令規定之相關福利 / 勞工退休金提撥 / 勞、健保

需求條件：

1. At least Bachelor degree in medical, nursing, or life science-related background
2. At least 1 year experience in submission
3. At least 2 year clinical contract/budget negotiation
4. Excellent communication and organizational skills
5. Work independently
6. With potential staffing management ability
7. Have site feasibility experience would be a plus

需求學位：

大學以上

管理責任：

不需負擔管理責任

工作時段：

日班

休假制度：

周休二日

需求人數：

1人

更新時間：

2019 / 05 / 17