Clinical Trial Monitor
Type:
Permanent
Location:
Brussels - Belgium, Brussels
Salary:
Depends on Experience
Advertiser:
Blue Lynx
Job Posted:
17th Nov 2008
Reference:
08-0360
Languages:
All of these languages are required. English
Dutch
French
All of these languages are required. English
Dutch
French
Job Description
For our international client, specialising in medical devises worldwide, we are currently looking for a Clinical Trial Monitor, to oversee their product trials in Belgium.
Job Profile
Based near Brussels and reporting to the Monitor Supervisor in Denmark, the Clinical Trial Monitor will have responsibility for clinical study activities related to monitoring functions, in conjunction with the study team members located in Europe and the USA. Key responsibilities will include:
Conducting periodic visits to investigative sites
Performing medical chart reviews
Verifying clinical trial study data
Coordinating the reporting of adverse event information
Assisting study teams with troubleshooting issues at site
Candidate Profile
Must be fluent in spoken and written French and English and fluency in Dutch or Flemish.
Must have a Degree in a Science, Nursing or Quality discipline
At least three years relevant experience in a clinical or hospital setting
Excellent communication skills and inter-personal skills
Organisational skills
Proven problem-solving skills
Ability to work on one’s own initiative within defined timelines
A high level of self-motivation
The successful candidate will be resident in, or willing to relocate to Belgium and be willing to travel extensively on company business as these roles will involve up to 80% travel within Belgium, and to the Netherlands and France. There may also be a necessity to work outside normal working hours
Current driving license
Our client offers excellent secondary benefits such as pension scheme, health insurance, 25 – 30 days annual leave and company car, laptop and mobile phone.
Your Career is Our Career
Our service is personal and targeted; we listen to what you want. Our ethos of "a good job well done", means that we work hard to deliver what we promise, each and every time. This focus allows us to provide customers with a total recruitment solution across discipline, level, location & requirement that combines a fresh approach with traditionally founded, tried and tested business principles.
Our experienced team of consultants will review your application and your CV in full. Candidates matching all vacancy requirements as specified by our clients will be contacted within five working days. If you have not been contacted, your application has not been successful on this occasion. Your CV will be forwarded to our admissions team who will be in touch with you to start/update your registration. If you are interested, please send your CV in English and in Word format.
Job Profile
Based near Brussels and reporting to the Monitor Supervisor in Denmark, the Clinical Trial Monitor will have responsibility for clinical study activities related to monitoring functions, in conjunction with the study team members located in Europe and the USA. Key responsibilities will include:
Conducting periodic visits to investigative sites
Performing medical chart reviews
Verifying clinical trial study data
Coordinating the reporting of adverse event information
Assisting study teams with troubleshooting issues at site
Candidate Profile
Must be fluent in spoken and written French and English and fluency in Dutch or Flemish.
Must have a Degree in a Science, Nursing or Quality discipline
At least three years relevant experience in a clinical or hospital setting
Excellent communication skills and inter-personal skills
Organisational skills
Proven problem-solving skills
Ability to work on one’s own initiative within defined timelines
A high level of self-motivation
The successful candidate will be resident in, or willing to relocate to Belgium and be willing to travel extensively on company business as these roles will involve up to 80% travel within Belgium, and to the Netherlands and France. There may also be a necessity to work outside normal working hours
Current driving license
Our client offers excellent secondary benefits such as pension scheme, health insurance, 25 – 30 days annual leave and company car, laptop and mobile phone.
Your Career is Our Career
Our service is personal and targeted; we listen to what you want. Our ethos of "a good job well done", means that we work hard to deliver what we promise, each and every time. This focus allows us to provide customers with a total recruitment solution across discipline, level, location & requirement that combines a fresh approach with traditionally founded, tried and tested business principles.
Our experienced team of consultants will review your application and your CV in full. Candidates matching all vacancy requirements as specified by our clients will be contacted within five working days. If you have not been contacted, your application has not been successful on this occasion. Your CV will be forwarded to our admissions team who will be in touch with you to start/update your registration. If you are interested, please send your CV in English and in Word format.

