Drug Safety Administrator

JOB-20241107-e299043e Drug Safety Administrator, Milton Keynes, England, £27,000 - £28,000 annually, full-time, dependent on experience We are seeking a skilled and motivated Drug Safety Administrator to join our dynamic team in Milton Keynes. This role offers an exciting opportunity to work at the forefront of pharmacovigilance, involved in the vital processes of reviewing, processing, and reporting adverse event data. Our company is known for its supportive environment and commitment to professional growth. Perks and benefits: As a valued member of our team, you'll enjoy several fantastic benefits that enhance your work-life balance and support your well-being. After successfully completing your probation, you will gain membership to our Private Healthcare Scheme, ensuring you have access to top-tier healthcare services. Enjoy the flexibility of hybrid working arrangements, allowing you to blend office and remote work in a way that suits you best. Access to exclusive corporate discounts means you can indulge in various products and services at great prices. Secure your future with our Company Pension Scheme and enjoy additional perks such as regular social events and professional development opportunities. What you will do: Participate actively in the collection, safety review, processing, and reporting of adverse event data in compliance with local and global regulations. Perform accurate computer data entry of adverse event information and ensure timely regulatory reporting. Assist the PV Manager in maintaining and updating standard operating procedures and working practices. Liaise with pharmaceutical companies and other business partners to ensure smooth communication and collaboration. Keep the Pharmacovigilance Manager informed of any issues related to products, adverse events, and other relevant areas. Upload ProQuest alerts for assigned active ingredients into the Literature Monitoring System, identifying key case reports and safety information. Process selected case reports and ensure proper MedDRA coding of adverse events. Conduct reconciliation with clients and PV partners, as required, and process reports from various sources in the drug safety database. Assess adverse events and perform listedness and causality assessments. Exchange PV case references with partners and follow up on direct reports from patients or healthcare professionals. Maintain Continued Professional Development to ensure up-to-date knowledge of medicinal products and industry regulations. Participate in team meetings and assist with documentation related to working practices and standard operating procedures. Life in Milton Keynes offers the perfect blend of big-city amenities and open green spaces. It boasts a wide range of leisure activities, excellent schools, and a diverse cultural scene. Come and join us in this vibrant community, where opportunities for growth and exciting experiences await! Working with Sanctuary Personnel: Sanctuary Personnel is a trusted and award-winning agency for roles. With an ‘Excellent’ rating on Trustpilot from over 1,000 reviews and many prestigious industry awards, we are dedicated to finding you the best possible rates in roles that match your skills and experience.

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