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Job Details

CLINICAL TRIAL / SAFETY ASSISTANT (Brussels, Belgium)

Company: Covance
Location: Brussels, Belgium
Reference: 24804
Closing Date: 07 Jan 19
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Our sponsor-dedicated team is rapidly growing in Brussels. We have a Clinical Safety Assistant job available, sponsor dedicated, office-based. This is a permanent job opportunity, ideally full time (the minimum we can consider is 0.8 FTE).

Requirements:

Clinical Safety Assistant. Pharmacovigilance administrative support.

Sponsor dedicated, office based, Brussels.

 

As an integral part of everything we do, our employees make a difference in the lives of millions of people… and you will too.

If you want to accelerate your Clinical Trials career think long-term and the possibilities we can offer you:

 

  • We have helped the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today and
  • 100 % of all Oncology drugs approved in 2016.

 

Explore this job as Clinical Safety Assistant with us and check for yourself why Covance has been named among the World´s Most Innovative Companies in Forbes´ 2017 Ranking, and more than 90% of the top 20 global pharmaceutical companies are repeat customers. 

 

Our sponsor-dedicated team is rapidly growing in Brussels. We have a Clinical Safety Assistant job available, sponsor dedicated, office-based. This is a permanent job opportunity, ideally full time (the minimum we can consider is 0.8 FTE).

Among other responsibilities, working closely with an international Safety/ Pharmacovigilance team, you will manage for your assigned cluster of countries:

  • Adverse Events
  • Serious Adverse Events
  • Suspected Unexpeted Serious Adverse Reactions
  • Develop Safety Update Reports
  • Translate essential document into 3 languages: French, Dutch and English

 

We will trust you to ensure that all the reporting regarding AEs, SAEs, SUSARs, etc., has been uploaded correctly at the appropriate databases and communicated on-time to all interested parties (CRAs, Global Safety teams, authorities, etc.

Our sponsor dedicated teams ensure that you will have a VARIED & DYNAMIC role, not rigidly fragmented in the same repetitive tasks day-after-day, forever …

We will help you achieve your goals by continuous training & professional development.

 

Education / Qualifications

  • You bring a High School Diploma or equivalent, preferred: Secretary/Medical Administrative.
  • You will work in an international environment, using English, French and Dutch in your day-to-day. You are able to attend to meetings, read, write and translate documents (such as medical records) in the 3 languages.

 

Experience

We need someone with min. 2 years experience working in clinical studies  as Clinical Trial Assistant, Project Assistant, in-house CRA, CRA who wants to stop travelling, etc.

Bringing specific experience in Pharmacovigilance managing AEs, SAEs etc., is a plus, not a `must´: with the above experience, we are keen to consider profiles interested in developing a career in pharmacovigilance reporting.

You are a hands on - team player- detailed- accurate-strong administrative/computer skills.

 

Apply for this job: CLINICAL TRIAL / SAFETY ASSISTANT (Brussels, Belgium)

Contact Information:

Address:  Covance- Brussels


Belgium
Tel: 
Fax: 
Website:  Visit Our Web Site

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