Med Info, Drug Safety & Pharmacovigilance Vacancies

Hendre Moolman at CK Clinical is currently recruiting for a number of Medical Information, Drug Safety and Pharmacovigilance jobs in the UK.

 

Please click on the links below to find out more and apply:

 

Medical Information Officer – Surrey, UK

 

Medical Information Officer – Surrey, UK

 

Medical Information Officer – Berkshire, UK

 

Senior PV Scientist (12 months) – London, UK

 

Pharmacovigilance Scientist – Hertfordshire, UK

 

Drug Safety Associate – Hertfordshire, UK

 

 

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Click here to register your CV online now >

 

Med Info, Drug Safety and Pharmacovigilance Vacancies - CK Clinical    Med Info, Drug Safety and Pharmacovigilance Vacancies - CK Clinical    Med Info, Drug Safety and Pharmacovigilance Vacancies - CK Clinical   Med Info, Drug Safety and Pharmacovigilance Vacancies - CK Clinical

 

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Drug Safety Associate Job based in Surrey UK

Hendre Moolman at CK Clinical is recruiting for a Drug Safety Associate to join a leading Pharmaceutical company in Surrey on a permanent basis.

Drug Safety Associate Job Description

As Drug Safety Associate you will participate in the delivery of a fully compliant pharmacovigilance system for the UK and ROI. Previous experience in Drug Safety, handling Spontaneous case reporting would be required.

Key Responsibilities:

  • Conduct all pharmacovigilance activities in compliance with regulatory guidelines and global and local SOPs
  • Receipt, processing and follow up of spontaneous adverse event reports
  • Review of medical information enquiries and quality complaints for presence of AEs
  • Processing of Argus reports received from Central DSP and onward reporting to Competent Authorities where appropriate
  • Receipt, review and onward reporting, as appropriate, to central DSP of MHRA ASPR reports
  • Reconciliation of medical enquiries, quality complaints and drug safety reports
  • Reconciliation of Medical Telephone Enquiry forms across Customer Services and Medical Affairs
  • Generation and/or completion of Monthly KPIs
  • Input into the continuous improvement of local pharmacovigilance systems including review of existing, and production of new SOPs
  • Maintenance of Summary of Pharmacovigilance Systems for NCH-UK
  • Generation of local PSURs for submission to MHRA and/or IMB
  • Generation of submission forms for global PSURs for submission to MHRA and/or IMB
  • Local literature searching
  • Local signal detection activities
  • Delivery of company wide AE training
  • Provide back up for responding to medical information enquiries
  • Develop product knowledge across NCH portfolio.
  • Deputise for Drug Safety Responsible Person as necessary
  • Handling of technical / quality complaints as necessary
  • Be nominated “Super User” of CRTS database for medical enquiries, technical (quality) complaints and drug safety reports and be responsible for the CRTS training of new starters within the department

 

As Drug Safety Associate you will have the following qualifications, skills and experience:

  • Life science or nursing graduate
  • Experience spontaneous case reporting
  • Experience with global safety databases
  • Experience using Volume 9A
  • Effective communicator both in writing and verbally
  • Excellent interpersonal skills
  • Able to operate as a flexible team player

 

How to apply:

Click here to apply online now.

For more information, please contact Hendre Moolman on 01438 870 023 or email hmoolman@ckclinical.co.uk.  . Please quote reference CL23522 in all correspondence.

Click here to search our current Drug Safety jobs now.

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Drug Safety Associate Job – Hertfordshire, UK

A global pharmaceutical company is looking for a Drug Safety Associate to join their team based in Hertfordshire, UK. The company are looking for candidates who are enthusiastic, have ambition and want to progress in drug safety.

Qualifications and experience:

  • Qualified pharmacist, relevant nursing qualification, life sciences degree or experience in drug safety
  • Previous exposure to Drug Safety is an advantage
  • Knowledge of drug safety regulatory obligations
  • Good knowledge of medical terminology
  • Ability to write clear, concise, unambiguous medical text
  • Ability to acquire knowledge in different disease and therapeutic areas
  • Fluent in English
  • Able to evaluate data and draw conclusions independently
  • Computer literacy essential

 

Attributes:

  • Able to take ownership of assigned cases
  • Conveys a sense of urgency
  • Proven good communication skills with an international perspective
  • Able to work under pressure
  • Confident decision maker
  • Willing to travel if required
  • Good time management
  • Flexible,able to interact well within a team setting
  • Good attention to detail

 

Apply now

For more information or to apply for this Drug Safety Associate role, please contact Krishna at CK Clinical on 01438 743 047 or email kpankhania@ckclinical.co.uk. Please quote reference CL21685 in all correspondence.

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