한국 노바티스에서 경력사원을 모집하고 있습니다.
노바티스 홈페이지(www.novartis.co.kr)를 방문하신 후 Job ID를 참조하여 지원하고자 하는 공고에 apply 부탁 드립니다.
지원하고자 하는 Job ID를 클릭하시면 Job Description을 보실 수 있습니다.
* CRA : 252853BR
**지원 방법** (꼭 시스템을 통하여 지원하셔야 합니다)
1. http://www.novartis.co.kr/ 홈페이지에 방문
2.우측 상단 채용 공고(BrassRing)을 클릭 후 지원하고자 하는 공고를 클릭 (지원하고자 하는 Job ID 참조)
* 시스템 이외의 방법으로 지원하신 서류는 반영되지 않습니다 *
**Job Description**
1. Participate in the process of identification and selection of investigators in col-laboration with clinical project leader.
2. Assume ambassadorial role to facilitate communication between sites and Key Novartis line functions to increase value proposition to investigators.
3. Facilitate preparation and collection of site level documents, especially ensure all document collected prior to study initiation.
4. Execute site initiation and training activities.
5. Perform monitoring visits according to monitoring plan.
6. Manage site drug supply management.
7. Resolve site level update of technical systems (Clin Admin, EDC).
8. Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc).
9. Manage recruitment implementing appropriate contingency plans at site level in col-laboration with clinical project leader.
10. Managing center specific master file, and ensure investigator file completed as required.
11. Assure continual GCP, ICH and Novartis SOP compliance (Informed consent process, Source data verification, AE and SAE reporting, IN, protocol, drug accountability etc.). Resolve deviations to standard by remedial action and training.
12. Author study monitoring reports/contact reports.
13. Perform data query resolution process (both at Site and with Data Management).
14. Execute site closeout activities.
15. May act as local clinical project leader, as assigned.
**Job requirements**
A degree in scientific or health discipline required and advanced degree preferable. Fluent in English & local language (Oral and written)
1. Basic medical and business knowledge.
2. Desired 2+ years experience in clinical research or having demonstrated adequate level of proficiency within the CRA I or II competency profile.
3. Understands and can apply knowledge of clinical trial designs to trial execution.
4. Basic understanding and experience in clinical development process including international standards (GCP/ICH), and local regulations.
5. Expertise in communication, managing multiple priorities and computer literacy.
한국 노바티스에서 경력사원을 모집하고 있습니다.
노바티스 홈페이지(www.novartis.co.kr)를 방문하신 후 Job ID를 참조하여 지원하고자 하는 공고에 apply 부탁 드립니다.
지원하고자 하는 Job ID를 클릭하시면 Job Description을 보실 수 있습니다.
* CRA : 252853BR
**지원 방법** (꼭 시스템을 통하여 지원하셔야 합니다)
1. http://www.novartis.co.kr/ 홈페이지에 방문
2.우측 상단 채용 공고(BrassRing)을 클릭 후 지원하고자 하는 공고를 클릭 (지원하고자 하는 Job ID 참조)
* 시스템 이외의 방법으로 지원하신 서류는 반영되지 않습니다 *
**Job Description**
1. Participate in the process of identification and selection of investigators in col-laboration with clinical project leader.
2. Assume ambassadorial role to facilitate communication between sites and Key Novartis line functions to increase value proposition to investigators.
3. Facilitate preparation and collection of site level documents, especially ensure all document collected prior to study initiation.
4. Execute site initiation and training activities.
5. Perform monitoring visits according to monitoring plan.
6. Manage site drug supply management.
7. Resolve site level update of technical systems (Clin Admin, EDC).
8. Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc).
9. Manage recruitment implementing appropriate contingency plans at site level in col-laboration with clinical project leader.
10. Managing center specific master file, and ensure investigator file completed as required.
11. Assure continual GCP, ICH and Novartis SOP compliance (Informed consent process, Source data verification, AE and SAE reporting, IN, protocol, drug accountability etc.). Resolve deviations to standard by remedial action and training.
12. Author study monitoring reports/contact reports.
13. Perform data query resolution process (both at Site and with Data Management).
14. Execute site closeout activities.
15. May act as local clinical project leader, as assigned.
**Job requirements**
A degree in scientific or health discipline required and advanced degree preferable. Fluent in English & local language (Oral and written)
1. Basic medical and business knowledge.
2. Desired 2+ years experience in clinical research or having demonstrated adequate level of proficiency within the CRA I or II competency profile.
3. Understands and can apply knowledge of clinical trial designs to trial execution.
4. Basic understanding and experience in clinical development process including international standards (GCP/ICH), and local regulations.
5. Expertise in communication, managing multiple priorities and computer literacy.