- 目录
第1篇 临床试验专员岗位职责
临床试验专员 position summary
80% fte of this position will support to clinical operation in ma function, 20% fte performs a variety of administrative support to ma senior director and ma team.
key responsibilities
1. clinical trial support
a. trial master file and other study related documents handling and archiving in office
b. clinical trial supplies logistic supporting and tracking
c. clinical trial contract including vendor contract management and supporting
d. clinical trial payment supporting and tracking
e. supporting on organize e_ternal and internal meetings, draft meeting minutes as needed
f. setup and maintain the database(s) in clinical operation as required
g. ma storage room management
2. admin support to ma senior director
a. arrange business trips, including the flight tickets and hotels and visa application as needed
b. logistic support for function visitor(s) in china including but not limited to visa application, hotel booking, administrative communication
c. function administrative file maintenance in ma
d. e_pense report and manage the reimbursement
3. office admin support to ma team:
a. assist internal process (e.g. prpo)
b. collect related information from team member and consolidate reports as needed, e.g. monthly report, etc.
c. function fi_ed assets management
d. assist in new comer on board process
e. be the contact person for department activities
f. assist on department meeting
skills and abilities
1. customer focus and good communication skill
2. good written and spoken english
3. result oriented and self-motivated
4. teamwork spirit
5. accountable with strong ownership
6. good command of ms skill (word, e_cel and powerpoint)
desirable
1. bachelor degree in relative disciplines, biomedical background is preferred
2. at least 2 years relative working e_perience
3. administrative e_perience in related clinical research ( international healthcare companies, or cros) is preferred
position summary
80% fte of this position will support to clinical operation in ma function, 20% fte performs a variety of administrative support to ma senior director and ma team.
key responsibilities
1. clinical trial support
a. trial master file and other study related documents handling and archiving in office
b. clinical trial supplies logistic supporting and tracking
c. clinical trial contract including vendor contract management and supporting
d. clinical trial payment supporting and tracking
e. supporting on organize e_ternal and internal meetings, draft meeting minutes as needed
f. setup and maintain the database(s) in clinical operation as required
g. ma storage room management
2. admin support to ma senior director
a. arrange business trips, including the flight tickets and hotels and visa application as needed
b. logistic support for function visitor(s) in china including but not limited to visa application, hotel booking, administrative communication
c. function administrative file maintenance in ma
d. e_pense report and manage the reimbursement
3. office admin support to ma team:
a. assist internal process (e.g. prpo)
b. collect related information from team member and consolidate reports as needed, e.g. monthly report, etc.
c. function fi_ed assets management
d. assist in new comer on board process
e. be the contact person for department activities
f. assist on department meeting
skills and abilities
1. customer focus and good communication skill
2. good written and spoken english
3. result oriented and self-motivated
4. teamwork spirit
5. accountable with strong ownership
6. good command of ms skill (word, e_cel and powerpoint)
desirable
1. bachelor degree in relative disciplines, biomedical background is preferred
2. at least 2 years relative working e_perience
3. administrative e_perience in related clinical research ( international healthcare companies, or cros) is preferred
第2篇 试验专员岗位职责
休闲试验专员 江苏楷益智能科技有限公司 江苏楷益智能科技有限公司,楷益 岗位职责:
休闲试验专员主要工作是加工试验各类膨化样品并研发新样品,以及膨化设备的安装调试。
任职要求:
工作态度积极,吃苦耐劳。有工作经验者优先。
第3篇 试验专员岗位职责试验专员职责任职要求
试验专员岗位职责
职责描述:
1.协助和参与临床试验方案的编写;
2.协助和参与临床试验中心的筛选、伦理资料等相关准备、递交以及召开伦理会议等工作;
3.负责临床试验项目的跟进，按要求检查临床试验项目的质量;
4.根据研究方案及公司sop要求，协助启动、监察和结束临床试验;
5.负责与cro公司及时沟通，确保临床试验工作顺利开展;
6.负责校对临床试验报告;
7.负责试验样品发放回收、登记、总结报告等工作，及时、准确地向上级报告临床试验过程中的重要事件，并协助完成临床文献检索及临床数据整理等工作;
8.其他上级主管分配的工作。
任职要求:
1.本科及以上学历，药学、临床医学等相关专业;
2.有临床监查和稽查经验，有骨科医疗器械临床试验经验者优先;
3.具备良好的沟通技能，英语四级以上;
4.需要经常出差。
