Facilitation organisation and completion of quarterly testing of different product families various implants completion of weekly water testing as well as quarterly Completion of reports and reviews with the data received from these tests Communicat
Providing medical and scientific evidence regarding our products to hospitals and healthcare professionals
My role focused mostly on headcount as my team was moving from a manual Excel process to a faster Power BI process I also helped with month end and quarterly financial tasks such as Journals and Balance Sheet Reconciliations Later in my placement I beca
I was placed within the EMEA oncology regulatory affairs team and worked on pharmaceutical submissions to health authorities as well as completing a regulatory research project throughout my year Day to day I was shadowing and working with regulatory pro
Supporting direct team with a wide range of RA related activities this included Requesting certificates to ensure products could be registered within markets analysing sales and forecast data supporting work related to MDR manipulating data within exc
Collating data and creating reports about them in a way that is more interpretable by the team and anyone who needs to use it Mine was more focused on OPEX and the spend of the UK amp IRL teams on their company cards
Timely track clinical study activities including emails compliance errors study meetings etc to use CTMS and vTMF to track files To present in core meetings and work hand in hand with Clinical Tesearch Associates and Principal Investigators
Designing custom made joint replacements for patients with unique needs
My role in the buisness unit finance team involved refreshing and maintaining financial reports for the team using different finance and reporting software planning budgets and managing spend with business partners and responding to ad hoc requests
I worked with all other marketing colleagues to execute a variety of projects My daytoday role therefore heavily involved communication about the status of a project along with planning the future activities to ensure the project stays on track I also
Managing the IT spending budget for the Europe Middle East and Africa region Working with financial statements data sources and excel Communicating with business partners on a regular basis to ensure with a following the company039s goals and objec
Supporting four clinical trials across two therapeutic areas Contributing to recruitment tracking data management trial master file maintenance and sample management Beyond my involvement in clinical trials I participated in the Bridge to Employment
Job responsibilities included 1 Ensuring all Individual Case Safety Reports ICSRs containing Adverse Events AEs were sent to Drug Safety in a timely manner 2 Compliancing all cases received for Product Quality Complaints PQCs and for the corre
Deal with multiple stakeholders for monthly billing Preparation of Journal and balance sheet reconciliations Internal compliance controls for month end tasks
As Marketing IP Student for DePuy Synthes I led and supported product demonstrations for internal and external audiences including surgeons and nurses To facilitate these workshops I was also responsible for inventory management raising purchase order
Main duties and responsibilities Inventory management Inventory accuracy Product storage layout and rationalisation to facilitate increased productivity and continuous improvement in inventory accuracy Inventory cycle counting across all franchi
Mostly my days consisted of completing tasks and responsibilities that are key to the sample management and tracking aspects of clinical trials These responsibilities usually ranged from weekly maintenance of patient samples crosschecked from a vendor d
Average daytoday activities included Leading relationship with the social media agency Supporting campaign PR and influencer activity Competitor analysis Performance analysis Website updates Updating Ecommerce assets
Activities surrounding the receipt of adverse event reports which includes entering data from the reports into a safety system As the year went on my day to day activities shifted more towards projects aimed at improving processes involved in adverse eve
Joining meetings with line manager and mentor to gain an understanding on the role Completing data review tasks from assigned clinical trials Meeting different colleagues from different departments through coffee connect and networking events Reading
