- 目錄
第1篇 臨床試驗專員崗位職責(zé)
臨床試驗專員 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 試驗專員崗位職責(zé)
休閑試驗專員 江蘇楷益智能科技有限公司 江蘇楷益智能科技有限公司,楷益 崗位職責(zé):
休閑試驗專員主要工作是加工試驗各類膨化樣品并研發(fā)新樣品,以及膨化設(shè)備的安裝調(diào)試。
任職要求:
工作態(tài)度積極,吃苦耐勞。有工作經(jīng)驗者優(yōu)先。
第3篇 試驗專員崗位職責(zé)試驗專員職責(zé)任職要求
試驗專員崗位職責(zé)
職責(zé)描述:
1.協(xié)助和參與臨床試驗方案的編寫;
2.協(xié)助和參與臨床試驗中心的篩選、倫理資料等相關(guān)準(zhǔn)備、遞交以及召開倫理會議等工作;
3.負(fù)責(zé)臨床試驗項目的跟進(jìn)，按要求檢查臨床試驗項目的質(zhì)量;
4.根據(jù)研究方案及公司sop要求，協(xié)助啟動、監(jiān)察和結(jié)束臨床試驗;
5.負(fù)責(zé)與cro公司及時溝通，確保臨床試驗工作順利開展;
6.負(fù)責(zé)校對臨床試驗報告;
7.負(fù)責(zé)試驗樣品發(fā)放回收、登記、總結(jié)報告等工作，及時、準(zhǔn)確地向上級報告臨床試驗過程中的重要事件，并協(xié)助完成臨床文獻(xiàn)檢索及臨床數(shù)據(jù)整理等工作;
8.其他上級主管分配的工作。
任職要求:
1.本科及以上學(xué)歷，藥學(xué)、臨床醫(yī)學(xué)等相關(guān)專業(yè);
2.有臨床監(jiān)查和稽查經(jīng)驗，有骨科醫(yī)療器械臨床試驗經(jīng)驗者優(yōu)先;
3.具備良好的溝通技能，英語四級以上;
4.需要經(jīng)常出差。
