Senior Patient Safety & Pharmacovigilance Scientist
at Boehringer Ingelheim LTD
Bracknell Forest, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 06 Oct, 2024 | Not Specified | 07 Jul, 2024 | 4 year(s) or above | Regulatory Requirements,Regulations,Pharmacovigilance,Communication Skills | No | No |
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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