GSK

I work as part of a small global team, supporting local patient affairs teams and playing a more strategic role in embedding patient advocacy and engagement (PA&E) across the company from R&D to commercial. I work with a wide range of internal and externa...

Pharmacovigilance is the science of detection, assessment, and identification of adverse drug reactions which occur in pharmaceuticals. Global Safety work to ensure the benefit-risk profile of a drug remains positive throughout its lifecycle, both in clin...

I work in a vaccines team. Initially I spent the first 7 months working solely on method development for a vaccine. The remaining time of my placement I helped out other analytical teams on large molecule projects and started another method development fo...

My role involves operational delivery of Managed Access Programs (MAPs) within GSK’s Oncology Medical Affairs Department. I coordinate drug access for investigational medicines, ensuring compliance with regulations, supply chain management, and vendor ove...

I usually spend a couple of hours in the lab performing experiments. Outside of the lab, I analyse the data from my experiments. I then write up the method, results, and conclusions of my experiments so the company keep a record of them. I also attend mee...

On a day-to-day basis, I am either in the lab doing an experiment, which typically takes a full day. Alternatively, I am analysing the flow cytometry results of an experiment which typically takes approx. a week. I sometimes have meetings or attend intern...

Lab duties; Registering materials Documenting experiments Prepping and running samples Team meeting Presenting findings Writing protocols Optimising workflows Working independently in the lab

Modification of existing and installation of new mechanical systems. Measuring parameters to correctly spec equipment and organisation of third party contractors. Understanding how modifications will affect the wider business including the planning of pro...

I'm part of the UK HR team, supporting the Policy and Immigration Manager in a dynamic role. In the Policy space, my responsibilities can include drafting new policies, refreshing existing ones, or managing flexible/home working requests. On the Immigrati...

My job role involves supporting multiple talent programmes and capability events for GSK's Global Finance team. Key projects are delivering Finance development days each quarter to upskill our Finance colleagues across areas such as digital, business acum...

My main responsibility was managing an external vendor to lead systematic literature reviews. I was an author, overseeing the process and ensuring that our work was reproducible. I was also delegated deep dives into literature for my team becoming an expe...

Each of GSK's potential products undergoes research and development which is a collection of studies in a project plan. For the project plans in my therapeutic area, I track and manage timelines and budgets for Non-Interventional Studies. This involves c...

- assisting in data management tasks for clinical studies - pulling information from veeva - completing trackers and other oversight tools - attending study meetings - performing QCs and kick off meetings - completing required study documents and working...

My work mostly consists of planning experiments, receiving DNA, transfecting mammalian cells to produce a protein, and then purifying it.

My role is a scientist trainee who would assist other scientist in their experiments. In the first three months, what I did mostly on a day-to-day basis are completing company training protocols, getting familiar with the labs and shadowing other senior s...

Synthesis of novel drugs and subsequent screening to assess for covalent modification. Half-lab based half data analysis

I have thoroughly enjoyed my placement here at GSK. The staff and management are all friendly and amazing to work with. My pay has been more than fair and I have received an additional yearly bonus too. Extra opportunities have been given for personal and...

My main role was troubleshooting machines and understanding why they broke. It involved completing investigations to prevent future downtime. I delivered change controls to ensure that mechanical changes could be implemented in a compliant way.

Facilities management

Day-to-day you will be involved in study team meetings to get an update on the status of the clinical trial. You will give updates on any progress made by the data management team, like how many data have been checked, if any queries have been sent to the...