临床助理--CTA for Chiltern (A Covance company )

Clinical Trial Administrator (CTA) performs study-relate******** asrequire******** the Department, including (but not limite********):communicate with Project Manager an******** of the project teamregarding study up******** maintain documentation as require********protocols, SOPs an******** stan******** to ensure timely production ofhigh quality clinical ******** provide system’s support, trackinformation relate******** the status of study activities an********with general administrative functions as required.

Clinical Trials Administrator- 1(Entry)
1. Documenting an******** study activities using relevant formsan********, as well as relevant Project Management System withguidance/support.
2. Assist in the preparation of study site files in accordance withrelevant SOPs.
3. Create an******** contact list of study team members, study s********an******** supplier******** organizations.
4. Assist with minute taking an******** for sponsor/external or internalteleconferences.
5. Assist in setting up an******** tracking systems for e.g. studysupplies an******** payments.
6. Assist in the tracking an******** of documents for all clinicalstudies into Chiltern’s global database.
7. Perform other duties as require******** the Department or ProjectTeam.
8. Liaise with all other Chiltern departments to ensure the smoothrunning of the study.

Clinical Trials Administrator- 2(Experienced)
1. Document an******** study activities using relevant forms an********,as well as Chiltern’s Project Management System.
2. Prepare study site files in accordance with relevant SOPs.
3. Create an******** contact list of study team members, study s********an******** supplier******** organizations.
4. Minute taking an******** documentation for sponsor or internalteleconferences.
5. Maintain tracking systems for study supplies an******** payments.
6. Assist in the tracking an******** of documents for all clinicaltrials into Chiltern’s global database.
7. Support Investigator Meetings.
8. May support in mentoring less experience******** on project ordepartment tasks an********.
9. Liaise with all other Chiltern departments to ensure the smoothrunning of the study.
10. Perform other duties as require******** the Department or ProjectTeam.

Clinical Trials Administrator- 3 (Senior)
1. Liaise with all other Chiltern departments to ensure the smoothrunning of the study.
2. Document an******** study activities using relevant forms an********,as well as Chiltern’s Project Management System.
3. Prepare study site files in accordance with relevant SOPs.
4. Create an******** contact list of study team members, study s********an******** supplier******** organizations.
5. Minute taking an******** documentation for sponsor or internalteleconferences.
6. Maintain tracking systems for study supplies an******** payments.
7. Support Investigator Meetings.
8. May support in mentoring less experience******** on project ordepartment tasks an********.
9. May assist the Line Manager with interviews for candidates for theCTA role.
10. Perform other duties as require******** the Department or ProjectTeam