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Drug Safety Specialist

  • Job type: Contract
  • Location: Basel
  • Salary: Competitive
  • Job reference: GRDL45G5
  • Sector: Safety, EPM Scientific, Quality
  • Date posted: 18/01/2018

A multinational Pharmaceutical company is searching for a Drug Safety Specialist to join their rapidly expanding site in the Basel area. 

My client is currently looking for senior consultants to work on a site on a consultancy basis to handle Adverse Events (AE) and Serious Adverse Events (SAE) reports in compliance with European and international regulatory requirements. My client is a global leader in projects.


Responsibilities:


- Reviewing and managing adverse-event case reports and submitting them to the relevant databases.
- Helps write and take charge of PSUR’s (Periodic Safety Update Reports) and the documentation and filing of them.
- Works to ensure compliance with case reconciliation and the notifying stakeholders
- Responsible for signal detection, evaluation and due diligence in response to regulatory safety inquiries.

Experience and Skill Requirements:


-  Experience within Pharmacovigilance
- Knowledge of local and global regulatory structures. 
- Experience with Safety documentation  
- Fluent in English.

What this Job Offers You:

- A high-level consultancy project working with a senior team of consultants on a difficult and interesting project. 
- Opportunity to work in a large multinational company with an exciting product.
- 12 month contract with the possibility of flexible working hours as the project develops.

How to Apply:

Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact Enquires(@)epmscientific.com or phone +442037588865


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