CRA / Clinical Research Associate
Join Pharmaxi as a Clinical Research Associate and support the delivery of clinical trials through site monitoring, documentation control and...
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Working in clinical trials is an opportunity to take part in projects that support the development of new therapies, medical devices and solutions for the healthcare sector. At Pharmaxi, we work with specialists from various areas of clinical research, offering opportunities for development in a CRO environment and participation in projects conducted in Warsaw and across Poland.
We are looking for people who want to develop their career in clinical trials, work well in a team and understand the importance of quality, timeliness and compliance with regulatory requirements.
We recruit specialists to work on clinical trials in areas such as monitoring, project management, regulatory affairs, data management, operational support and collaboration with sponsors and investigational sites. Below you will find current job opportunities at Pharmaxi, including roles related to CRO work, clinical project coordination and documentation management.
Join Pharmaxi as a Clinical Research Associate and support the delivery of clinical trials through site monitoring, documentation control and...
See moreJoin Pharmaxi as a Clinical Trial Assistant and support project teams in the day-to-day organisation of clinical trials. This position...
See moreJoin Pharmaxi as a Project Manager and take responsibility for coordinating clinical trials at different stages of project delivery. This...
See moreJoin Pharmaxi as a Regulatory Affairs Specialist and support the preparation and management of regulatory documentation for clinical projects. This...
See moreWorking at Pharmaxi gives you the opportunity to take part in national and international clinical trial projects in an environment focused on quality, responsibility and professional development. We value clear rules of cooperation, well-organised processes and practical support at every stage of project delivery.
Depending on the position and scope of responsibilities, we offer opportunities to expand your competencies, participate in training, work with experienced specialists and develop in a selected area of clinical research. Partnership-based communication, mentoring, knowledge sharing and a friendly team atmosphere are important to us.
Clinical trials also create opportunities for cooperation with physicians, pharmacists and other healthcare professionals. Their expertise may be important in the analysis of medical documentation, subject-matter support for the team, coordination of activities at sites and oversight of selected project elements.
People with medical or pharmaceutical education can develop in areas related to trial conduct, document review, cooperation with sponsors, communication with investigational sites and support for processes compliant with GCP requirements and regulations applicable to clinical trials.
For people starting a career in the clinical research industry, internships and traineeships can be a good way to understand CRO work from the operational, administrative and project perspective. They provide an opportunity to gain first experience, become familiar with clinical trial documentation and understand how cooperation between the sponsor, investigational site and project team works.
We invite students, graduates and people who want to develop in areas such as clinical trial assistant, data management, regulatory affairs, project support or clinical trial coordination to contact us.
A career in clinical trials can begin with roles supporting the project team, such as Clinical Trial Assistant, clinical trials department assistant, junior data management specialist or project administrative support. Accuracy, responsibility, good organisation, knowledge of English and willingness to learn procedures and regulatory requirements are important in this work.
Over time, you can develop towards clinical trial monitoring, project management, regulatory affairs, data management or other specialisations related to the conduct of clinical projects. Experience gained in a CRO helps you better understand the entire clinical trial process – from preparing documentation and working with sites to overseeing quality and timely project delivery.
The application process is simple. Choose a job offer that matches your experience and career plans, then submit your CV using the form or the indicated contact address. After reviewing your application, a recruiter or the person responsible for the relevant recruitment process will contact you.
The next stages may include a recruitment interview, discussion of your experience, scope of responsibilities, expectations and possible cooperation. At every stage, we try to clearly inform candidates about the process and next steps.
If you do not currently see a position that matches your experience, you can send us your CV. We are happy to get to know people interested in working in clinical trials, CRO, monitoring, project management, regulatory affairs, data management and operational project support.
Your application may be considered in future recruitment processes when an opportunity appears that matches your competencies and professional development direction.
