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Senior Surveillance Specialist

Michael Page Technology
Job LocationCambridge
EducationNot Mentioned
Salary400.00 - 420.00 per day
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeTemporary , full-time Work from home

Job Description

  • Manage applicable tools, documentation and methodologies to ensure processes and systems fully address the needs of organization.
  • Lead and coordinate routine system maintenance activities (e.g. MedDRA, WHODD, Ontology updates)
  • Contributes to the development of procedures, work instructions, system specifications related to the use of Patient Safety Technical Solutions owned information sources and toolsets.
Client DetailsMy client - a critical health care organisation in the Pharmaceuticals industry are looking for a Senior Surveillance Specialist- join their site in Cambridge remotely on an initial 12- month contract!DescriptionThe successful candidate for the Senior Surveillance Specialist - Pharmaceuticals industry 12 month contract role will fulfil the following responsibilities -
  • Manages applicable tools, documentation and methodologies to ensure processes and systems fully address the needs of organisation.
  • Lead and coordinate routine system maintenance activities (e.g. MedDRA, WHODD, Ontology updates)
  • Contributes to the development of procedures, work instructions, system specifications related to the use of Patient Safety Technical Solutions owned information sources and tool sets
ProfileTo be considered for the Senior Surveillance Specialist - Pharmaceuticals industry 12 month contract role based in Cambridge/ remote the candidate must present evidence of the following:
  • Bachelors degree in a scientific discipline
  • Significant experience in pharmacovigilance with proven record of supporting safety tools / solutions.
  • Proven competence, with extensive involvement in the successful design, delivery, validation, deployment or maintenance of information/systems solutions in support of safety.
  • Experience in working across different geographic locations, organisations, and cultures.
  • Excellent interpersonal and communication skills with ability to efficiently communicate with all levels of the organisation.
  • Knowledge of the procedures, processes and standards governing clinical trial data (documents and data) with health authorities worldwide, and experience of implementing these within the business.
  • Higher degree in a clinical or safety-related discipline.
  • Microsoft Office Suite
  • Business Objects experience (desired)
Job Offer
  • 12 month contract with a world renown pharmaceutical client
  • Remote working
  • Hourly rate of up to £420 p/day outside IR35 via UK Ltd

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