As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

We are currently looking for talented Clinical Research Associate or Senior Clinical Research Associate to join our team

In this role, you will work directly with one of our renowned key sponsors, supporting them and your assigned study sites during phase I - III of clinical trials. You will have a direct impact on the development of innovative medications, improving the lives and health of patients every day. If you are looking to broaden your therapeutic expertise whilst gaining exposure within a world class pharmaceutical working environment, this is an excellent opportunity!

What we have to offer:

flexible working hours, capped overtime and compensatory time off in lieu
highly competitive compensation packages
regular, merit-based salary adjustments
lunch allowances on work days
extensive medical coverage under our insurance plan
flexible car allowance policy
excellent training and career development opportunities as well as support with furthering your education
strong support from Line Management and more than 20'000 colleagues worldwide
the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years

Your main responsibilities:

Perform required monitoring tasks at your study sites in an efficient manner, according to SOPs and established guidelines; prepare accurate and timely trip reports and own all aspects of study site management as described in the project plans
Ensure the study staff conducting the protocol receive all materials and instructions to safely enter patients into the study
Protect study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by diligently reviewing source documents and monitoring the data for missing or implausible entries
Generate queries and resolve issues according to data review guidelines on Fortrea or sponsor data management systems
Act as a central point of contact for clinical trial suppliers and other vendors supporting your studies
Own the entire process of Serious Adverse Event (SAE) reporting pertaining to your studies

Education & Experience:

Degree in a relevant field such as life sciences, (veterinary) medicine, pharmacology, biology, chemistry, health care, health management, nursing, etc.,
First professional independent site monitoring experience as a Clinical Research Associate
Familiarity with applicable Slovak and international regulatory requirements such as GCP / ICH
Working knowledge of Microsoft Word, Excel and PowerPoint
Effective time management and organizational skills and a keen attention to detail
Ability to establish and maintain effective, trustful working relationships with diverse internal and external stakeholders
Business fluency in Slovakian - both spoken and written - as well as a good command of English are a must

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit .

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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