Posts Tagged ‘Pharmacovigilance Specialist’

Our Latest Pharmaceutical Jobs – 17th of September 2012

Monday, September 17th, 2012

Looking for a job in the Pharmaceutical Industry? Please click on the links below to find out about our latest pharmaceutical jobs new in this week:

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Clinical Project Manager – Switzerland

Pharmacovigilance Officer – Belgium

Expert Clinical Manager – Switzerland

Data Analyst Statistician

Drug Safety:

Medical Information Officer

Medical Development Advisor – South East

Pharmacovigilance & Clinical Trial Administrator

Pharmacovigilance Specialist

Clinical:

Field Based Senior CRA, Oncology

Clinical Support Specialist – North East

Regulatory Affairs:

Regulatory Affairs Leader – Mauritius

Medical Writer/Regulatory Doc Scientist – Hertfordshire

Meeting Planner – Hertfordshire

Associate Director, Reg Affairs, CMC

Medic:

Medical Affairs Manager – Oncology – South East

 

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Once registered, one of our specialist Pharmaceutical Recruitment Consultants will be in contact to discuss your requirements and any relevant pharmaceutical jobs we are recruiting for at the moment. Good luck with your job hunt

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Drug Safety Specialist Contract Job in Cambridgeshire

Wednesday, March 14th, 2012

Hendre Moolman at CK Clinical is recruiting for a Drug Safety Specialist to join a leading pharmaceutical company in Cambridgeshire, UK. This is a contract position.

As a Drug Safety Specialist you will participate in the day-to-day functioning of the Drug Safety QC division. You will perform quality control checks on cases entered on the global safety databases, collating findings from QC checks and performing monthly review on sample of cases.

In addition, as Drug Safety Specialist you will have the following responsibilities:

  • Work under general guidance of Manager using well defined procedures
  • Perform quality control (QC) checks on cases entered on the global safety database and provides feedback to case owners
  • Collate findings from QC checks in order to identify areas for clarification with respect to data entry conventions and specific training needs
  • Perform monthly review on sample of cases not submitted to regulatory authorities in order to confirm reporting decisions
  • Seek assistance from appropriate internal and external resources

As Drug Safety Specialist you will have the following qualifications and experience:

  • Ability to maintain confidentiality, quality and accuracy
  • Understand safety database structures and is familiar with data retrieval tools
  • Demonstrate attention to detail, teamwork and initiative
  • Must be proficient in email and verbal communication
  • Proficient in Microsoft Excel, Power point and Word
  • BSc degree in Life Sciences, Pharmacy, Nursing and minimum 2 years of relevant drug safety experience

 

How to apply:

Click here to apply online now.

For more information regarding this Drug Safety Specialist position, please contact Hendre Moolman at CK Clinical on 01438 870 023 or email hmoolman@ckclinical.co.uk. Please quote reference CL23871 in all correspondence.

Click here to search our pharmaceutical jobs in Cambridgeshire now.

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