Senior Patient Safety & Pharmacovigilance Scientist

at  Boehringer Ingelheim LTD

Bracknell Forest, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate06 Oct, 2024Not Specified07 Jul, 20244 year(s) or aboveRegulatory Requirements,Regulations,Pharmacovigilance,Communication SkillsNoNo
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Description:

WHY THIS IS A GREAT PLACE TO WORK

Boehringer Ingelheim has been recognised as a Top Employer in the UK. Being certified as a Top Employer confirms our dedication to a better world of work, delivered through excellent HR policies and people practices. To learn more visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work

REGULATORY AND / OR ORGANISATIONAL REQUIREMENTS

  • Extensive knowledge of the regulatory requirements in the UK, Ireland and Malta
  • Sound knowledge of ICH-GCP

REQUIREMENTS

  • Minimum of 4 years experience within Pharmacovigilance
  • Good understanding of regulations pertaining to Pharmacovigilance.
  • Demonstrate a good knowledge of PV Safety databases and complete tasks in a timely manner in accordance to BI procedures
  • A team player at all levels, supporting others, sharing expertise and ideas.
  • Excellent attention to detail with a ‘can do’ attitude and ensuring positive working relationships with stakeholders
  • Excellent presentation and communication skills, along with good prioritisation and organisational skills
  • Demonstrate continuous proactivity and be solution orientated
  • Life Science degree or Health Care Professional desirable

How To Apply:

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Responsibilities:

  • Support and mentor the PSPV team to prioritize workload and to identify areas of learning and share solutions focused ideas with PSPV management
  • Have a compliance overview of the local PV activities performed by the local PSPV scientist(s)
  • To monitor the relevant regulatory websites for the UK, Ireland, Malta and the responsible territories and to update the Regulatory Intelligence System accordingly.
  • Provide support for PSPV audit and inspections and any type of PSPV non-compliances
  • Provide support to ensure appropriate PV language is include in the relevant contracts.
  • Support the PSPV physician to increase awareness of RMP related information
  • Develop strong cross-functional relationships through PSPV awareness activities.
  • Providing in-person or virtual AE training to appropriate stakeholders
  • Maintain a strong working knowledge of relevant PV legislation, regulations and company procedures.
  • Proactively contributing to process improvements.
  • Ensure BI Business partner and external customer communications are handled promptly and professionally.


REQUIREMENT SUMMARY

Min:4.0Max:9.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Bracknell Forest, United Kingdom