Starting out as a CRA: Martina’s Story
Starting a career in clinical research can feel both exciting and overwhelming. For Martina Tesi, the journey into becoming a Clinical Research Associate was shaped not only by professional ambition, but by the people and support system she found along the way.
Originally from a small town in Tuscany, Martina officially became a CRA in November 2025. Her path into the industry began with a specialised Master’s degree in Clinical Research at the University of Florence, following an earlier experience as a Research Fellow in a pre-clinical Pharmacology Laboratory.
Martina joined ICON in June 2025 as an In House CRA, stepping into an entirely new professional environment with curiosity and determination.
Building confidence through collaboration
One of the most significant milestones in Martina’s early career came just a few months after joining ICON. During September 2025, she successfully completed the 10 accompanied visits required for CRA certification under Italian law.
For Martina, this period was about much more than ticking off a professional requirement.
“I had the opportunity to work alongside colleagues that suddenly became friends, who are absolutely trustworthy and professional on the job.”
The experience reinforced something that quickly became clear throughout her first months at ICON: collaboration and inclusion are deeply embedded within the culture.
From day one, Martina found herself surrounded by colleagues willing to guide and support her as she adjusted to the fast paced world of clinical research. She also credits her mentors for helping her grow in confidence as she continues to develop in her role as a junior CRA.
“Inclusion was the basis of every relationship I managed to build, and I am glad to realise that I always had any kind of help whenever I needed it.”
Growing personally and professionally
Transitioning into a new industry can often come with steep learning curves, but Martina describes her growth at ICON as something she never expected to happen so quickly.
She highlights the support she received from both her manager and teammates as a defining part of her experience.
“From the very beginning, I felt encouraged, supported, and guided, which allowed me to integrate quickly and confidently into the team.”
Just as importantly, Martina felt that her enthusiasm and motivation were recognised and genuinely valued.
For her, that recognition reflects a workplace culture where people are encouraged to contribute, develop, and succeed together.
Why teamwork matters in clinical research
Clinical research is known for being dynamic and demanding. Priorities shift constantly, timelines can be challenging, and workloads often evolve quickly.
Martina believes teamwork is what makes navigating those challenges possible.
“In such a demanding and fast paced environment, effective collaboration, mutual support, and open communication are essential to maintain focus, manage workload, and ensure both high quality performance and personal sustainability.”
Looking ahead
As Martina continues her career journey as a CRA, she remains grateful for the opportunities, mentorship, and support she has found at ICON plc.
Her story is a reminder that career growth is not only about gaining technical expertise. It is also about finding an environment where people feel supported, included, and empowered to succeed together.
Sign up for post alerts
ICON & You
The potential of together.
Careers that improve the lives of patients, our clients and each other. Are you ready to make a difference?
View jobsRelated jobs at ICON
Salary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Project Management
Job Type
Permanent
Description
As a Trial Delivery Management (Advanced) at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives.What You Will Do:You will m
Reference
JR152627
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
As a Trial Master File (TMF) Lead at ICON, you will be responsible for overseeing the Trial Master File (TMF) management processes, ensuring compliance with regulatory requirements and best practices
Reference
JR152546
Expiry date
01/01/0001
Author
Rita VillavicencioAuthor
Rita VillavicencioSalary
Location
United States of America
Location
Canada
Multiple US Locations
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Project Management
Job Type
Permanent
Description
Reporting to the Director of Feasibility, the Feasibility Principal provides strategic, study-level feasibility leadership within the Patient and Site Engagement (PSE) team, supporting the acceleratio
Reference
JR152872
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
US, Blue Bell (ICON)
Location
Florida
Blue Bell
Miami, FL
Tampa, FL
Orlando, FL
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This is a sponsor dedicat
Reference
JR152866
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittRelated stories
Teaser label
Our PeopleContent type
BlogsPublish date
05/26/2026
Summary
From Data Management to Leadership For Sajna Basant, a career in Biometrics has always been about more than data. “Data is not just numbers,” she explains. “It represents real people, their health
Teaser label
IndustryContent type
BlogsPublish date
05/18/2026
Summary
How Clinical Project Managers Keep Complex Trials Moving Forward linical trials are becoming more complex than ever. Global study footprints, evolving regulations, increasing data demands, and tigh
Teaser label
Our PeopleContent type
BlogsPublish date
05/14/2026
Summary
From Mystery Novels to Medical Breakthroughs For Savannah Muccia, problem-solving is more than just part of the job. Whether she is reviewing clinical trial data or reading a suspense-filled myste
Recently viewed jobs
Salary
Location
China, Beijing
Location
Beijing
Chengdu
Guangzhou
Shanghai
Tianjin
Wuhan
Xi'an
Dalian
Changsha
Hangzhou
ShenYang
Zhengzhou
Nanjing
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Assitant at ICON, you will play a pivotal role in assisting with the design and analys
Reference
JR136660
Expiry date
11/12/2026
Author
Irena GuoAuthor
Irena GuoSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Belfast
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Quality Assurance
Job Type
Permanent
Description
As an Operations Quality Specialist at ICON, you will support the development and implementation of initiatives and established processes that support operations in maintaining inspection readiness. T
Reference
JR150876
Expiry date
05/14/2027
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
France, Paris
Location
Paris
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Corporate Support
Job Type
Permanent
Description
As a Contract Analyst I at ICON, you will prepare, verifying, and carrying out invoicing via electronic processing and reporting activities for an assigned portfolio of accounts. What You Will Do:You
Reference
JR149671
Expiry date
04/24/2027
Author
Serena MilanesiAuthor
Serena MilanesiSalary
Location
Poland, Warsaw
Location
Warsaw
Gdansk
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:
Reference
JR148436
Expiry date
06/02/2027
Author
Michal CzyrekAuthor
Michal CzyrekImpactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON