Medical Admin Assistant I
About the role
This vacancy has now expired. Please click here to view live vacancies.
Job Title: Medical Affairs Assistant
Location: Warsaw, Poland - office based
At ICON, it's our people that set us apart.
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry! Are you one of them?
At ICON, we have an incredible opportunity for a Medical Affairs Administrator to join our team in Warsaw, Poland.
The Medical Administrative Assistant I will maintain efficient and accurate daily work flow of documents (paper & electronic) and information within Medical Affairs (MA) department and will provide administrative support to MA departmental staff as required.
The Job:
- Provide Administrative Support for Medical Monitors and Medical Affairs Specialists (MAS)
- Prioritize and schedule project meetings as directed by MM and MAS, including preparation and distribution of presentations, agendas, reserving conference rooms, coordinating materials for distribution, insuring technical facilities setup prior to start of meetings, etc.
- Produce accurate, complete and professional correspondence, including meeting minutes, as assigned within designated timelines across project meetings (i.e. MM monthly team meetings, PRMs, etc.)
- Coordinate setup of required systems during study startup (mailboxes, distribution lists, fax numbers, Tracking tools, etc.) as they apply to MA tasks
- Maintain tracking systems during active study period (i.e. eligibility, laboratory reports, ECGs, etc.) as required within assigned studies
- Schedule and track project review meetings
- Maintain project training records as required
- Maintain electronic / paper SSP binders as necessary
- Ensure regularly scheduled maintenance of MIMS for assigned projects
- Work with MAS to develop File Management plan for assigned projects
- Lead all aspects of filing maintenance in TMF and eTMF (ICOMaster, Y:Drive, or sponsor-specific system) for assigned projects
- Assist Medical Affairs team with obtaining and filing eSignatures for required study documents
- Oversee archiving and scanning activities at study closeout
- Completion, including submission, of expense reports for MA team members
- Assist with travel preparations for bid defense and project specific meetings, e.g., insure that all applicable forms are completed per ICON policies and procedures for business travel
- Manage and maintain administrative tasks as they pertain to coverage of 24/7 Emergency Medical Monitor system
- Assist with audit preparations as requested by MA team members
Experience:
- Good verbal and written communication skills
- Proficient in English (verbal and written)
- Basic computer skills (Microsoft Office applications, specifically Word, Excel, Visio, and PowerPoint)
- Attention to detail
- Good organizational and time management skills
- Knowledge of medical terminology
- Familiarity with standard office equipment (copier/printer, fax)
- Ability to work as part of a team
Why join us?
Other than working with an outstanding team of ambitious people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
Ongoing development is vital to us, and as a Principal Medical Writer, you will have the opportunity to progress your career, with the potential to move into other related areas to improve your skillset. Our benefits package is competitive, our scope is international, and we sincerely care about our people and their success.
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.
EOE race/colour/religion/sex/sexual orientation/gender identity/disability/vet/national origin
Impactful 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
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
10/08/2025
Summary
A Career Built on Purpose: Dimitar's Journey at ICON Plc Dimitar Karzhin’s career path is not one he could have predicted. What began with a decade as a practicing General Practitioner in Bulgaria l
Teaser label
Career ProgressionContent type
BlogsPublish date
09/19/2025
Summary
How to Build a Strong LinkedIn Profile That Attracts Employers LinkedIn is no longer just a digital CV. It is a professional network, a space to showcase your skills and a platform to connect with
Teaser label
Our PeopleContent type
BlogsPublish date
09/16/2025
Summary
Growing with ICON: Christina’s Journey in Clinical Operations and Quality Leadership At ICON, we are proud to showcase the incredible journeys of our colleagues who make a real impact on pati
Similar jobs at ICON
Salary
Location
Poland, Warsaw
Location
Sofia
Budapest
Warsaw
Bucharest
Johannesburg
Madrid
Reading
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
Role Summary:Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation in accordance with ICON SOPs/WPs,
Reference
JR137577
Expiry date
01/01/0001
Author
Persis DavisAuthor
Persis DavisSalary
Location
Malaysia, Kuala Lumpur
Location
Kuala Lumpur
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking a Senior Investigator Pricing Analyst to join our diverse and dynamic team. As a Senior Investigator Pricing Analyst at ICON, you will be essential in developing and analyzing
Reference
JR134880
Expiry date
01/01/0001
Author
Sitti LimAuthor
Sitti LimSalary
Location
Regional United States (PRA)
Location
Montreal
Multiple US Locations
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Medical Writing
Job Type
Temporary Employee
Description
This role supports clinical trial transparency and disclosure activities, including document redaction, results posting, and plain language summary development, in compliance with global regulations a
Reference
JR137668
Expiry date
01/01/0001
Author
Brendan HoeyAuthor
Brendan HoeySalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Scientist
Job Type
Permanent
Description
We are currently seeking a Clinical Scientist to join our diverse and dynamic team. As a Clinical Scientist at ICON, you will play a critical role in designing and conducting clinical studies that adv
Reference
JR136282
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Operations
Job Type
Permanent
Description
What you will be doing:Services/deliverables include the management of all documents and logistical and administrative tasks related to trial feasibility, start-up, execution and close out of clinical
Reference
JR137635
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
What you will be doing: The L-LTM role will be accountable/responsible for ensuring top-quality end-to-end trial delivery at a country level, managing the consistency of Local Trial Management duties
Reference
JR137619
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica Hawkins