Covance

Assistant, Drug Safety

Job Location(s) KR-Seoul
Job Number
2021-61128
Job Category
Drug Safety/Pharmacovigilance
Position Type
Full-Time
Telecommute
No

Job Overview

Are you ready to discover you next career at Covance?
 
A career at Covance provides our employees the unique chance to create an immediate impact and difference in our patient’s lives. Joining Covance will offer a rewarding career, a chance to work in an energetic & team oriented work place, and access to competitive benefits. With the support of exceptional people from across the globe and a vast array of career options, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. As a Covance employee, your work will be meaningful, the patient outcomes are real, and the results are lasting.
 
Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.
 
As a Drug Safety / Pharmacovigilance(PV) Assistant you will be assisting the local operational drug safety activities and have participate in the performance and success of the growing team in Korea.
Your responsibilities will be to:
- Assist in or complete per the Safety Management Plan (SMP) the processing of all adverse event reports from any source
- Assist in producing queries of safety data for clients as appropriate
- Assist in the generation and maintenance of the PSS metrics
- Assist Data Management or clients on reconciliation of safety databases
- Provide input for monthly status reports
- Maintains a comprehensive understanding of Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance
- Possess knowledge of other procedural documents, e.g., SOPs, and how they impact safety
- Build and maintain good PSS relationships across functional units
- Demonstrate role-specific Core Competencies on a consistent basis
- Demonstrate company Values on a consistent basis
- Assist in the preparation of client meetings and liaise with clients where appropriate
- Assist with the set-up of, and the provision of data to, Safety Committees/DSMBs
- Any other duties as assigned by management
Education/ Qualifications
- Non-degree + 3-4 yrs relevant experience** (or 1 yr safety experience)*
- Associates Degree + 2-3 yrs relevant experience** (or 1 yr safety experience)*
- Associate degree RN + 1-2 yrs relevant experience**
- Degree preferred (but not necessary) to be in one or more of the following disciplines: Biological Sciences, Pharmacy, Nursing, Life Sciences, and Chemistry.
 
*Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions
 
**Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance
 
- High degree of accuracy with attention to detail
- Functions as a team player
- Good communication
- Good written and verbal communication skills
- Ability to work independently with moderate supervision
- Good keyboard skills with knowledge of MS Office and Windows application would be beneficial
- Experiences in translating source documents from Korean to English & English to Korean
- Experience in Argus system

Education/Qualifications

- Non-degree + 3-4 yrs relevant experience** (or 1 yr safety experience)*
- Associates Degree + 2-3 yrs relevant experience** (or 1 yr safety experience)*
- Associate degree RN + 1-2 yrs relevant experience**
- Degree preferred (but not necessary) to be in one or more of the following disciplines: Biological Sciences, Pharmacy, Nursing, Life Sciences, and Chemistry.
 
*Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions
 
**Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance

Experience

- High degree of accuracy with attention to detail
- Functions as a team player
- Good communication
- Good written and verbal communication skills
- Ability to work independently with moderate supervision
- Good keyboard skills with knowledge of MS Office and Windows application would be beneficial
- Experiences in translating source documents from Korean to English & English to Korean

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