Job Description
Due to continued growth we are currently seeking an additional Pharmacovigilance Officer to join our team in a well-established Consultancy. The position involves supporting the activities within the Pharmacovigilance areas of the company encompassing drug safety.
This is an entry level role, you would be a science graduate maybe with some work experience but it could be a first role for the right candidate as training will be provided. You will however need to demonstrate ambition to continually develop together with a drive to innovate and be part of a growing company in the pharmaceutical space.
A covering letter detailing why you believe you are the right candidate in addition to your CV will be required for applications to be considered. Applications close on 21st April 2023.
Key Duties and Responsibilities
- Pharmacovigilance activities including weekly literature searching, preparation of safety reports, reviewing PVOR’s (Pharmacovigilance Obligation Report) and reporting ADR’s (Adverse Drug Reaction) where required.
- Receiving and responding to medical information enquiries.
- Proof reading product safety information including Summary of Product Characteristics (SPC’s) and Patient Information Leaflets (PILs), and preparation of user tests.
Role Requirements
- Graduate in a Science based subject.
- Excellent verbal and written communication skills with high level of attention to detail and accuracy of work.
- Strong organisation skills and ability to cope with large volume of work across different areas of the company with changing deadlines.
- Ability to work well both alone and as part of a team.
Behavioural Competence
- Customer Focus: Manages your own activities to ensure they are focussed on delivering outstanding service to the end customer.
- Teamwork: Can work well in a multi-disciplinary team and across teams to deliver requirements of role.
- Flexibility: Able to adapt to meet the needs of the business at any point in time.
Package Details
Competitive graduate level salary commensurate with experience, Annual performance related bonus, Contributory Pension, 25 days annual leave, East Midlands Office based minimum 2 days per week but flexible hybrid working arrangements available.
About Us
The Callisto Pharma Group has grown from the formation, in 2003, of Callisto Regulatory Consulting Ltd, which provided regulatory and technical support to pharmaceutical manufacturers to the current group of companies that provide a complete range of technical services across the whole supply chain to multiple regulated sectors including human, veterinary and herbal medicines, borderline products, biocides, medical devices and food supplements.
We work across the UK, Europe, and the rest of the world for Clients operating in highly regulated sectors, ranging from global multi-nationals to single product licence holders.
We are committed to investing in our people and infrastructure which enable us to be highly flexible, efficient and innovative in our services to Clients.
Job Types: Full-time, Permanent
Schedule:
Application question(s):
- Have you included a covering letter with your application?
Education:
Work authorisation:
- United Kingdom (required)
Work Location: Hybrid remote in Derby, DE74 2QF
Application deadline: 21/04/2023
Reference ID: CAL2023-1-PV
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