LMS Case Management Specialist - Student Placement in High Wycombe

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Duration: 12 months

Location: High Wycombe, Buckinghamshire (Moving to Maidenhead in Oct 2026)

LMS Case Management Specialists collect and evaluate information from patients and healthcare professionals to try and identify new information about the use of medicines and any side effects experienced by patients. Safety monitoring of medicines is a continuous process, performed during clinical trials when medicines are developed, once medicines are launched and throughout the entire period where a medicine is available for patients to use. The team is the first point of contact within the company for incoming adverse event reports. The department also monitors our pharmaceutical products across their lifecycle, from clinical trials through to post-marketing surveillance, to detect, assess, understand and prevent adverse events. The team works to evaluate drug efficacy and maintain patient safety. You will join our Pharmaceutical business as a LMS Case Management Specialist and will be given a high level of exposure to many aspects of the Pharmacovigilance division. This is an office‑based role with global reach working with colleagues from around the world.

Main Duties And Responsibilities

• Receipt and processing of incoming safety information from multiple sources and countries, both internal and external to the Company
• Responsible for the collection, review and reporting of Adverse Events (AEs) and pregnancy reports obtained through spontaneous reporting, solicited reports, clinical study, Local Health Authorities (LHAs) and other potential sources
• Assist with initial quality review and assessment of individual cases
• Provision of safety information/acknowledgement to marketing partners/other third‑party partners/Global Medical Safety within the internal and contractual timelines
• Co‑ordinate/perform the follow‑up of missing information from the AE reporter
• Working with colleagues from around the world on multiple projects, developing strong project management and leadership skills
• Assist in the provision of local data as required supporting the preparation of Safety Summary reports (PSURs, ASR, etc.)
• Assist in the quality review of data captured in the Global Safety Database
• Ensure that day‑to‑day Pharmacovigilance functions are performed satisfactorily and that full regulatory compliance is maintained at the Local Operating Company (LOC) level
• Accurate and timely documentation of deviations to process/timelines, including root cause analysis and documentation of Corrective and Preventive Actions (CAPAs)
• Support all occurrences of internal and external audits and inspections
• Support the onboarding activities of placement student successors
• Working cross‑functionally with internal teams globally
• Collaborating with the student cohort on fundraising and charity events

Requirements Of The Role

• 2 years of degree level study completed
• A minimum of 2:1 achieved in first year of study
• Science degree types only

Key Skills And Competencies

• High level of accuracy and attention to detail
• Passion for working in the pharmaceutical industry
• Excellent communication skills both written and oral
• Seeks opportunities to learn and grow professionally
• Able to prioritise and manage own workload autonomously
• Flexible and adaptable team player
• Self‑motivated
• Actively seeks feedback, appreciates and uses constructive criticism
• Bounces back quickly from mistakes; learns and moves on quickly