- Experience Level
- Experienced (non-manager)
Responsibilities in the role include:
- Post-marketing Pharmacovigilance will include Safety management, Medical review of ICSRs, safety database and medical coding.
- Clinical Safety encompasses the medical review of trial documents in the preparation of projects and at the culmination of the projects, medical review of data listings, validation of medical clinical study data, premature discontinuation cases and protocol deviations.
- Risk assessment during trials and management of queries regarding medical issues during data cleaning.
- Signal and Risk management and writing of RMPs.
- Medical Project Management during clinical trials.
We are looking to speak to Medics or Pharmacists who are located in Poland and looking for their next career step. The client is open to part Home Working after probation is completed.
To discuss this in more detail please contact Julie Robinson on +44 1293 584300 or firstname.lastname@example.org
Salary: On application
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