Drug Safety Scientist

CHF95 - CHF100 per hour
  1. Interim/Contract
Basel
  1. PVG & Drug Safety, Drug Safety Writing
Posted: 11/11/2019
BBBH12763

This vacancy has now expired. Please see similar roles below...

Hobson Prior currently have an exciting opportunity for a Drug Safety Scientist to join a Swiss international healthcare organisation who are focused on offering medical solutions in order to transform patients' lives. As the Drug Safety Scientist, you will support the safety risk management of assigned products across the lifecycle including early and late phase development safety activities as well as safety activities for marketed products.

Job Responsibilities:

  • In collaboration with the safety science product you will be responsible for aggregate case reporting activities and aggregate reporting (e.g., DSUR, PBRER).
  • Accountable for signal detection and management activities including, including respective documentation and drug safety reports.
  • Coordinates and assists in Health Authority interactions and responding to requests.
  • Contributing to risk management activities including preparation and maintenance of CCDS, labeling document maintenance, risk communications, RMP, REMS.
  • Contributing to study management through cross-functional teams and document review across the development continuum (early phase to post marketing studies), including PASS.
  • Interfacing with business process owners on processes executed by Safety Science.
  • Responsible for supporting processes involving safety science.
  • Responsible for carrying out activities related to quality system management for safety science.

Key Skills:

  • Able to work with remote partners and teams across global sites.
  • Excellent communication skills, both written and verbal.
  • Fluent in English.

Requirements:

  • Bachelor's degree in healthcare related field or equivalent experience (minimum).
  • Work experience in pharma safety, pharmacovigilance or other related pharmaceutical development area of at least 2 years.
  • Appreciation of GVP and GCP and regulated processes and end to end clinical trial lifecycle.
  • Understanding on application of data analysis / statistical methods to evaluate, interpret and present scientific data with clarity.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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