Freelance Clinical Site Auditor
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Brabant Flamand Belgium.
The client is an internationally established pharmaceutical company
ROLE DESCRIPTION
The client is looking for a well experienced auditor who can perform audits for their clinical investigative sites worldwide. The project will be for a period of a year and requires full fte. Besides traveling to the client's clinical investigative sites worldwide, you can partly work from home as well.
RESPONSIBILITIES
- You will examine documents related to the clinical trial activities
- You will determine if these activities are compliant with the SOP's and GCP regulations and other safety requirements
- You will travel twice a month (depending on the number of audits) to the clinical investigative sites within and outside Europe to perform site audits
REQUIREMENTS
- Minimom of 5 years auditing experience in the pharmaceutical industry
- Knowledge and work experience with GCP regulations
- Previous work experience with clinical trials in the pharmaceutical industry
- Good understanding and communication of the English language is a must and Dutch is a pre
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Kimberley Rijnbeek.
Opis stanowiska
SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Brabant Flamand Belgium.
The client is an internationally established pharmaceutical company
ROLE DESCRIPTION
The client is looking for a well experienced auditor who can perform audits for their clinical investigative sites worldwide. The project will be for a period of a year and requires full fte. Besides traveling to the client's clinical investigative sites worldwide, you can partly work from home as well.
RESPONSIBILITIES
- You will examine documents related to the clinical trial activities
- You will determine if these activities are compliant with the SOP's and GCP regulations and other safety requirements
- You will travel twice a month (depending on the number of audits) to the clinical investigative sites within and outside Europe to perform site audits
REQUIREMENTS
- Minimom of 5 years auditing experience in the pharmaceutical industry
- Knowledge and work experience with GCP regulations
- Previous work experience with clinical trials in the pharmaceutical industry
- Good understanding and communication of the English language is a must and Dutch is a pre
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Kimberley Rijnbeek.
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Kontrola jakości
