The success story of Emanuela (Italy)
She spent the next seven years developing her skills and experience as a Clinical Research Associate, before moving into Project Management activities in 2006. Emanuela spent over eleven years with her previous employer, before applying to CROMSOURCE for a Senior Clinical Project Manager position. Following the interview process, she was impressed and interested in our company, in particular because of our company environment and mission.
She is now in a sponsor dedicated role, managing one large study in rare disease and paediatrics, with several sites across Europe, Israel, Serbia and North America. She is in charge of managing the CRO involved to conduct the study and all study stakeholders. Activities include monitoring the study budget and providing input in cost proposal reviews.
She feels proud of being able to help and to gain the trust of the sponsor and the study team, and to contribute effectively to the project, seeking out and recommending process improvements.
Her goal is to contribute to CROMSOURCE’s growth and make a difference, playing a real role inside the organisation.
The success story of Fanny (Belgium)
Fanny obtained her degree in Philosophy and initially had no idea about clinical research.
When looking for a job she came across a vacancy for Clinical Trial Assistant with CROMSOURCE and decided to apply. She started with us in August 2008 in a sponsor dedicated role with a large pharma company and changed sponsor in 2011 initially in the same role, but in 2014 moved into the role of Senior Clinical Trial Assistant. In 2015 she moved into a different area, taking a role as Material Coordinator Associate, and was promoted in 2016 of Distribution Material Coordinator.
Having started from scratch, after 10 years of hard work, she was promoted to Senior Distribution Material Coordinator in December 2018. A great achievement!
She is now performing the oversight of depots within distribution network. On one hand she has to ensure the general oversight of all material movement (finished goods) to sites from Hubs and Depots and on the other hand, she has to ensure compliance of activities performed adhere to EU and Belgian regulatory requirements, with GMP/GDP’s and with the company corporate requirements.
Finally, she is sometimes also involved in special projects supporting the development and implementation of distribution strategies related to products and capacities.
The success story of Monique (The Netherlands)
After finishing her degree, Monique started working in Belgium and spent 8 years there working in an academic environment and some time in a clinical research environment. In 2015 she decided to move back to the Netherlands.
She started her job search and reached out to the CROMSOURCE team. She had several conversations with different team members, who gave her a good feeling and made her feel welcome. CROMSOURCE introduced her to one of the top 10 pharmaceutical companies for a CRA position in the Netherlands, and following several positive interviews and thanks to the great support received from CROMSOURCE, things turned out well. After a recruitment and hiring process of less than 2 months, Monique officially joined CROMSOURCE as a CRA in 2015.
After working as a CRA for 2.5 years, in the same sponsor dedicated position, she was promoted to Clinical Study Manager. In this role, she looks after Neurology and Ophthalmology studies and also serves as the Neurology/Ophthalmology counterpart for the respective Medical Affairs Department. She is an important link between Clinical Operations and Medical Affairs for these indications.
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