Clinical Research Associate II, Poland

We are currently recruiting for the position of Associate Clinical Trial Manager in Poland for a global leader in the diagnostic and medical industry. The person in this role will be part of the Clinical Trials Team, responsible for the planning, execution, management, and closure of projects related to the company's clinical trial plans. A key part of the...

Job Description As a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. You will conduct onsite monitoring visits and be responsible for site communication and...

Requisition Number7944Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...

The position As Clinical Research Associate your role is to verify the accuracy and completeness of the trial data, that the rights and well-being of human subjects are protected, and the conduct of the trial follows the current approved protocol, GCP and local legislations. As a CRA, you will be representing Novo Nordisk and being the main point of...

Are you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or...

The Clinical Trial Associate (CTA) plays a critical role in supporting clinical research projects, ensuring smooth coordination, administration, and documentation of clinical trials. This role ensures compliance with all regulatory and company guidelines.Team: SRSSponsor: You will be dedicated to a global pharmaceutical/biotech leader in innovative drug...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond...

We are currently recruiting for a Clinical Trial Associate for a global leader in diagnostics/medical industry. This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support. If you already have at least one year of experience in clinical trials and have advanced English...

IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. ...

Requisition Number8201Employment Type:Regular Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. ...

The Site Budget and Contract Lead (SBCL) leads the development of investigator budget and contract proposals. The SBCS acts as the main point of contact for budget and contract negotiations for investigator sites across North America, EU and other countries, as applicable and Sponsors. The SBCS will be responsible for all project activities related to...

The Site Budget and Contract Lead (SBCL) leads the development of investigator budget and contract proposals. The SBCS acts as the main point of contact for budget and contract negotiations for investigator sites across North America, EU and other countries, as applicable and Sponsors. The SBCS will be responsible for all project activities related to...

Are you looking for an opportunity where you can utilize your medical knowledge to communicate scientific data and to interact with medical thought leaders? Are you passionate about the world of clinical trials? Are you highly motivated by being able to make a difference to improving patients’ lives? If so, you should continue reading and apply today! ...

Our team is growing, join us on our mission to drive healthcare forward! What We Offer / USPs The chance to work on cutting edge medicines at the forefront of new medicines development IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and...

The Project Director is responsible for oversight of the conduct of a program or portfolio of clinical studies or large global multicentered trials with large study budgets. The portfolio may comprise studies for specific customers, and/or a group of studies within the same therapeutic area or indication for more than one customer. The Project Director...

Associate Project ManagerICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We currently have an exciting new opportunity for an Associate Project...

Informacje o ofercie pracyIntego Group’s office in Warsaw, Poland, is currently seeking students and graduates from local universities to join our internship program.The clinical research industry is a rapidly growing field that leverages cutting-edge data science and biostatistics to improve healthcare outcomes. In our Clinical SAS® Internship Program,...

Job Description Take your career to the next level and lead challenging full-service global clinical research projects, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study. Your responsibilities will include: Management of global, multi-center clinical research projects in a variety of...

Requisition Number8135Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...

Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week This role sits within the Clinical Document Anonymisation and Data Sharing function in Clinical Trial Transparency, Chief Medical Office. The Clinical Trial Transparency leads the AstraZeneca Group of Companies,...