Build structured knowledge of safety monitoring, SAE/SUSAR reporting and safety processes across the clinical trial lifecycle.
Start the program on the AIDIFY platform with a learning area subscription.
Complete the 10 program courses one by one and collect a certificate for each of them.
Finish all 10 courses to earn the job-ready certificate.
Aleksandra is a pharmacist with many years of experience in pharmacovigilance. After graduating, she joined Pfizer as a Junior Safety Data Management Specialist working in the Hub supporting all European countries, Middle East and Africa where she gained experience in case processing activities, triage and acceptance of reports coming from Eudravigilance database and submission to Ethics Committees and Investigators. Currently she manages a team of safety specialists.
Along with her weak spot for the literature cases she is also keenly interested in signal detection.
Passionate about further broadening of her knowledge she regularly participates in numerous trainings, e.g. ‘Signal and Risk Management in Pharmacovigilance MasterClass’ in November 2020, organized by Global Leading Conference, ‘Safety Data Exchange Agreements (SDEAs) and PV Arrangements with External Vendors’ in May 2022, postgraduate studies “Management and Monitoring of Clinical Trials” in 2019 at Kozminski University.
Knowing that her work has an impact on health and safety of patients is the greatest motivation and gives her a lot of satisfaction.
When she is not working you can usually meet her cycling or playing squash. She is also interested in learning different languages as they help her to explore new cultures around the world.
Hello there! I'm Marek, a seasoned lawyer with a deep-rooted interest in drug safety. I'm delighted to welcome you to our top-notch AIDIFY platform where we aim to enrich your understanding of the Pharma industry.
I have devoted years of my career to understanding and navigating the complex world of pharmaceutical regulations, with a strong emphasis on pharmacovigilance. This unique intersection of law and drug safety has offered me a distinct viewpoint, one that I am eager to share with you.
As a proud member of the Polish Society of Pharmacovigilance, I'm continuously updating my knowledge and understanding of the industry's intricacies, keeping myself aligned with the latest trends, regulations, and safety practices.
Having served in various Pharma companies over the years, I've acquired not just theoretical knowledge, but also a wealth of practical insights. I firmly believe in blending theory with practice, which allows me to offer you a balanced and comprehensive learning experience.
Join me on this educational journey, where I aim to equip you with a well-rounded understanding of pharmacovigilance and its legal aspects. Let's shape your future in the Pharma industry together. Your journey with me begins now.
Hello! I'm Monika, a seasoned professional in the Pharma industry, and I'm thrilled to welcome you to my SME page on the AIDIFY platform.
With over 15 years in the field, serving as the Head of Country Pharmacovigilance in a major global pharma company and as the Vice President of the Polish Society of Pharmacovigilance, I've gathered a wealth of knowledge and experience that I'm eager to share with you.
In my roles, I'm directly involved in setting industry standards and keeping my finger on the pulse of the latest trends, thanks to leading the Pharmacovigilance working group in Infarma. I've honed the ability to break down complex concepts into easily understandable lessons, an asset that will serve you well on this educational journey.
As a co-author of the 'Pharmacovigilance Guide', I've laid out comprehensive expertise in print. Now, through this e-learning platform, I look forward to directly engaging with you, sharing my insights, and helping you reach new heights in your career.
Join me, let's broaden your horizons together in the Pharma industry. Your journey starts now.
Excellent communicator with can-do attitude and strong desire to learn. Project Manager with line management responsibilities focused on quality. Currently fulfilling the role of an Oversight Portfolio Manager working on a governance level, responsible for several studies of one client and oversight and support a group of CTMs allocated for those projects. Client oriented and dedicated team player. Long-term goal is to have an independent and responsible position as a global project director. Experience in pharmaceutical marketing, medical affairs and clinical trials gained in pharma companies and CROs.Founder and member of Polish Pharmaceutical Students’ Association. Member and head of the training group at Polish Association for Good Clinical Practice (GCPpl). Pharmacist with strong interest in clinical pharmacy. Academic teacher delivering lectures related with clinical trials.
Certificates: Soft Skills Trainer Certificate, Prince2 Foundation Training Certificate, Barnett GCP Certificate. Laureate and winner of a 3rd place of the national competition “Leaders of Clinical Trials (2021)” in the category Project Manager. Scholar of Leslaw A. Paga Foundation in the program “Healthcare Leaders”.
Privately foodie and enthusiast of cooking, travelling and fantasy books.
She has been involved in the clinical research industry since 2015. She currently works for a global pharmaceutical company as a Manager in the Clinical Documentation team, where her main role is FSO Operations Lead.
She places high value on personal development and the quality of performed activities, which makes her a valued member of project teams. She has operational experience gained in global CROs and pharmaceutical companies. She has worked on both investigational and medical device projects in a variety of therapeutic areas.
From the very beginning of her work in clinical research, she has struggled with the complex nature of clinical trial documentation and TMF, which she continues to explore to this day.
In addition to her day job, she is actively involved in the academic community, initially as a coordinator and support to the manager of a post-graduate study in the clinical trial area. Currently, she is a lecturer at Conducting and Monitoring Clinical Trials and Associate Director in Third Party Processes & Operations.
This collaboration started after the previously completed postgraduate studies in Conducting and Monitoring Clinical Trials. Graduate of Nicolaus Copernicus University in Torun in the faculties of molecular biology and environmental protection.
Although she started her professional life at the Central Forensic Laboratory of the Police, she now finds herself perfectly at work in clinical project activities and now she is conducting other types of investigations.
2 active offers
€6,190 / month
Company: Advantage Technical Agency
Offer language: English Posted:20 days agoEst. €6,080–8,630 / month
Company: REQ Solutions Agency
Offer language: English Posted:24 days agoGet 10 courses and a job-ready certificate in one focused program, included in the Clinical Trials learning area subscription.
