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[Janssen] Clinical Research Associate

  • Titolo [Janssen] Clinical Research Associate
  • Funzione R&D
  • Sottofunzione Clinical Trial Administration
  • Località Yongsan-gu, Seoul, South Korea
  • Data di pubblicazione
  • Riferimento 2306112689W
Fai Domanda Ora


Johnson & Johnson is the world's most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world's most pressing health issues.

1. 포지션: Clinical Research Associate
2. 계열사: 한국얀센 (Janssen) 
3. 근무지: 서울시 용산구
4. 근무 형태: Regular

A Site Manager I (SM I, Clinical Research Associate) serves as the primary contact point between the Sponsor and the Investigational Site.  A Site Manager I is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure. Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities. The Site Manager I will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols.  May contribute to process improvement and training. 


1. Acts as primary local company contact for assigned sites for specific trials. 
2. May participate in site feasibility and/or pre-trial site assessment visits 
3. Attends/participates in investigator meetings as needed. 
4. Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other 
reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies. Responsible for the implementation of analytical risk based monitoring model at the site level and to 
work with site to ensure timely resolution of issues found during monitoring visits. 
5. Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases. Responsible in close collaboration with LTM and central study team for the activities during site activation phase in order to speed up the process and activate the site in shortest possible timeframe. 
6. Contributes  to  site  level recruitment strategy  and contingency  planning and  implementation  in partnership with other functional areas. 
7. Ensures site study supplies (such as Non-Investigational Product (IP), lab kits, etc.) are adequate for trial conduct. 
8. Ensures that clinical drug supplies  are  appropriately  used,  handled  and stored  and  returns  are accurately inventoried and documented. LD Version 1.0 dated 18 October 2017 (FINAL) 
9.  Arranges for the appropriate destruction of clinical supplies.
10.  Ensures site staff complete data entry and resolve queries within expected timelines.
11. Ensures accuracy, validity and completeness of data collected at trial sites
12. Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs )/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate.  For 
AEs/SAEs, ensures that they are consistent with all data collected and with the information in the source documents.
13. Maintains complete, accurate and timely data and essential documents in relevant systems utilized for trial management. 
14. Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter in accordance with the SOPs.  Promptly communicates relevant status information and issues 
to appropriate stakeholders. 
15. Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times. 
16. Collaborates with LTM for documenting and communicating site/study progress and issues to trial central team. 
17. Attends regularly scheduled team meetings and trainings. 
18. Complies with relevant training requirements.  Act as local expert in assigned protocols. Develops therapeutic knowledge sufficient to support role and responsibilities. 
19. Works closely with LTM to ensure Corrective Action Preventative Action (CAPA) is completed for Quality  Assurance  (QA)  site  audits  and  for  quality  issues  identified  at  the  site  during  routine 
monitoring and other visit types, e.g. On Site Quality Monitoring Visit (OSQMV). 
20. Prepares trial sites for close out, conduct final close out visit. 
21. Tracks costs at site level and ensure payments are made, if applicable. 
22. Establishes and maintains good working relationships with internal and external stakeholders in particular investigators, trial coordinators and other site staff. 
23. May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as required/appropriate. 
24. Acts as a point of contact in site management practices. 
25. May contribute to process improvement and training.
This is not an exhaustive, comprehensive listing of job functions.  May perform other duties as assigned. 

Principal Relationships:

Primary Reporting Structure:  Reports to a Functional Manager 
Primary interfaces:  Functional Manager, CTA, LTM and CTM.
Other Internal Interfaces:  R&D Country Head, Therapeutic Area Manager/Physician, Quality & Compliance Manager/Specialist, Training Manager, Contracts & Grants, Local Drug Safety Officer (where required) and Site Manager team. 
External Interfaces: Investigators and their delegates at site (trial site personnel.)


  • A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required. 
  • A minimum of 1 year of clinical trial monitoring experience is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility. 
  • Specific therapeutic area experience may be required depending on the position. 
  • Strong working knowledge of GCP, company SOPs, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines. 
  • Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.  
  • Proficient in speaking and writing the country language and English. Good written and oral communication


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