Clinical Standards IT Platform Engineer

This position will be responsible for delivering AZ end-to-end Clinical Analysis and Reporting Standards in the area of A&R (raw data standards to SDTM mapping, support/management SDTM and ADaM standards within the metadata repository) with quality and timelines, following established standards and processes. Provides solutions for analysis and reporting...

The Associate Director Standards Developer is primarily responsible for leading the technical development, management and maintenance of AZ end-to-end Clinical Analysis & Reporting Standards activities in their area of expertise ( clinical coding, clinical dictionaries, and data analysis & reporting standards (SDTM, ADaM, TLFs)) with quality and timeliness,...

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 Opportunity For our Abbott Electrophysiology Division (EP) we are currently looking for a well-skilled person to join our clinical team in Poland as a Field Clinical Engineer. This is a fully field-based role, requiring daily traveling across assigned territory: zachodniopomorskie, lubuskie area, with a preferred home location - Szczecin. ...

We are looking for a Senior Data Analyst to join the RITS and our client - one of the leading pharmaceutical companies.RITS Software House, part of the RITS Group, is a leading IT company specializing in software development. We offer high-quality services dedicated to both the Polish and international markets. Our company is part of one of the...

Location: Warsaw, hybrid work (3 days from the office, 2 days from home/weekly) .NET Software Engineer/ IT Platform Engineer , primarily an individual contributor who will pair with other Software Engineers, Leads, and Architects to design, build, test and deploy software solutions. The role will be involved in analysing requirements, implementing...

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...

Senior Scientist , Clinical Informatics Location: Barcelona, Spain; Warsaw, Poland Competitive Salary & Benefits Make a more meaningful impact to patients’ lives around the globe Here you’ll have the opportunity to make a meaningful difference to patients’ lives. With science at its heart, this is the place where breakthroughs born in the...

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...

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...

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! ...

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...

SECURITAS GROUPStrongly united by the purpose “We help make your world a safer place”, Securitas successfully integrates technology, people, and knowledge to offer protective services to clients all over the world. Securitas offers security services by combining expertise in on-site, mobile, and remote guarding with electronic security and experience in...

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,...

PPD, part of Thermo Fisher Scientific, is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose to improve health!  We are vital links between an idea for a new medicine and the people who need...

At GSK, we want to supercharge our data capability to better understand our patients and accelerate our ability to discover vaccines and medicines. The Onyx Research Data Platform organization represents a major investment by GSK R&D and Digital & Tech, designed to deliver a step-change in our ability to leverage data, knowledge, and prediction to find new...

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...

Job Overview The Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of a program of assigned clinical supply chain projects. The Clinical Supply Chain Manager will support the ongoing development and optimization of the Clinical Trial Supplies department and processes. Essential Functions Interpret clinical...