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 Giuseppe (Italy)
Giuseppe obtained a degree in Medicinal Chemistry and Pharmaceutical Technology, but it wasn’t until he ventured into the post-graduate Master at ISTUD Business School that he fell in love with clinical research.
After a 7-month traineeship at another CRO, Giuseppe joined CROMSOURCE in July 2019 as a Clinical Trial Administrator in a sponsor-based dedicated role. He was intrigued by this chance to work in clinical research as a dedicated resource to a pharma company.
In this role, he had the chance to start developing his skills towards a career in project management. He managed several trackers, was responsible for patient recruitment, reviewed CRA monitoring visits reports, communicated with Principal Investigators and attended some remote site initiation visits.
In November 2020, Giuseppe transitioned into a new role within CROMSOURCE internal full-service team, as a Project Coordinator. In this role, he will continue to grow in project management to become in charge of managing clinical projects.
With this new position he now has the chance to experience both the sides of the industry, having worked in a clinical department of a pharmaceutical company and now working in clinical operations with a CRO.
Giuseppe feels lucky to have been able to quickly grow and progress and make a start towards fulfilling his dream of becoming a Clinical Project Manager.
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