LMS Case Management Specialist - Student Placement

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. Learn more at https://www.jnj.com

Job Function:
Career Programs

Job Sub Function:
Non-LDP Intern/Co-Op

Job Category:
Career Program

All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom, Maidenhead, Berkshire, United Kingdom

Job Description:

Drug Safety – Local Medical Safety (LMS) Case Management Specialist – Student Placement 2026  

 

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, it is performed during clinical trials when medicines are developed, once medicines are launched (also called ‘licenced’) 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, in order to detect, assess, understand and prevent adverse events.

Ultimately the team works to evaluate drug efficacy and maintain patient safety.

You will join our Pharmaceutical business in the role of 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.

This is an exciting and unique opportunity to be at the forefront of drug development in one of Europe’s fastest growing top ten pharmaceutical businesses.

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...