？ Knowledge of the protocols through knowledge of the examinations procedures in connection with the Study Nurse position as discussed in the protocols in accordance with the study specific defined responsibility log. ？ Thorough knowledge of CCBR procedures quality control regulations (relevant fthe Study Nurse position), which forms the basis of performing clinical studies. ？ Knowledge of international/national regulations instructions fperforming clinical studies. ？ Perform in a professional, kind efficient manner, when taking care of study participants. ？ Thorough knowledge to the content of the Study File responsible fthe document filling. ？ Have a good grasp of the Patient File. ？ Responsible fthe content of the Patient File, general pages as well as study specific pages. ？ Responsible fcoordination concerning eligibility in the study enrolment phase. ？ study staff members on current study procedures other relevant information. ？ Make appointments with Sponsors representative fmonitoring. ？ Always be updated on the current study status. ？ Thorough knowledge of the time schedule. ？ Handling of drug supplies. ？ Handling of test results. ？ Last check of Patient Files CRF’s. ？ To participate in add information to planned clinic meetings. ？ To participate in education training planned by CCBR. ？ To participate in arrangements planned by CCBR, with the purpose of nurturing the solidarity between individual demarcation groups collaborating groups. ？ To participate in subject recruitment program/community out reach. ？ Participate in meetings arranged by Study Management Manager/GM; such as investigatmeetings, initiation meetings etc. 职位福利：五险一金、绩效奖金、交通补助、餐补、通讯补助、带薪年假、定期体检、节日福利
更新于 2024-11-19
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