Fadumo joined Immedica in 2023. Here, Fadumo reflects on the journey so far, sharing insights into the role, everyday work and how the experience of growing with the company has shaped both professional development and perspective.
 
What does a typical workday look like for you?  
A typical day consists of internal project meetings and meetings with external partners, as well as planning upcoming projects  and managing timelines. 

What are your main responsibilities during the day? 
Preparing Marketing Authorization submissions, variations  and responding to questions from regulatory authorities. 

Which part of your job do you enjoy the most? 
What I really enjoy about my role is how broad it is and the  opportunity to work across different countries and regions.  No days are the same, and I appreciate working closely  with experienced colleagues and partners, especially in the  area of rare diseases. 

What is the biggest challenge in your role?
Given the dynamic and evolving regulatory landscape, staying up to date with changing regulations can at times be challenging, particularly in a global role. 

How does your work contribute to Immedica’s mission?  
Every new Marketing Authorization approval is a vital part of bringing Immedica’s medicines available to patients worldwide and supporting our mission. Knowing the impact this work we are doing has on patients’ lives is a strong source of everyday motivation. 

What advice would you give to someone who wants to work in a similar role within the pharmaceutical industry? 
Be curious and open to learning. To be successful in Regulatory Affairs requires strong communication skills, a broad perspective, and attention to details. 

What do you enjoy doing when you are not working? 
When I’m not working, I enjoy spending my time with my family and training at the gym.