Clinical Application Expert

As a Clinical Research Expert at TN Poland, you will be responsible for providing expert guidance on regulatory matters and ensuring compliance with complex regulatory issues and projects.Responsibilities:Conduct regulatory intelligence gathering to support development of regulatory roadmaps.Author and maintain documentation to sustain regulatory...

Site Name: Warsaw, PolandClinical Writer ExpertThe Clinical Writer Expert is responsible for delivering high-quality written content to support the company's mission. This role involves working independently or collaboratively with teams to draft, review, and approve written assignments. The ideal candidate will have a strong understanding of clinical trials...

Job Title:Field Clinical Engineer, ElectrophysiologyLocation: Łodź area, Warsaw, PolandJob Category:OtherEU Work Permit Required:YesThe OpportunityWe are seeking a skilled Field Clinical Engineer to join our Abbott Electrophysiology Division (EP) team in Poland.This fully field-based role requires daily travel across the assigned territory (Łódź...

Job OverviewAt PSI CRO AG, we are seeking a highly skilled Clinical Data Expert to join our team. This role will play a crucial part in our centralized monitoring efforts, ensuring the highest quality of data and insights.Key Responsibilities:Participate in the selection of Risk-Based Monitoring (RBM) systems and provide training to project teams and...

Social network you want to login/join with:Clinical Application Specialist Healthcare Informatics, Warsawcol-narrow-leftClient:PhilipsLocation:Warsaw, PolandJob Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:6d6b9cbf3f8cJob Views:5Posted:19.03.2025Expiry Date:03.05.2025col-wideJob Description:JOB DESCRIPTIONJob TitleClinical...

Job SummaryWe are seeking a skilled Clinical Development Medical Review Expert to join our team. As a key member of the Oncology Clinical Development organization, you will be responsible for ensuring the medical consistency and integrity of clinical data.Main ResponsibilitiesData Review and Interpretation: Responsible for reviewing and interpreting clinical...

R&D Procurement: Driving Efficiency and InnovationJob OverviewThis position involves leading the Clinical Services category at GSK, pushing the boundaries of what is possible through the application of advanced procurement techniques and strategic partnerships. Ideal candidates possess extensive experience in procurement, contract negotiation, and supplier...

We're a privately owned company that values its employees and invests in their professional development and success. Our company overview highlights our commitment to quality and excellence.Role ResponsibilitiesThe Clinical Data Scientist will report to the Clinical Data Science Manager and Centralized Monitoring, working with clinical trials patient and...

Clinical Sales Representative at Boston Scientific GruppeClinical Sales Representative - Rhythm ManagementAbout the Role:We are seeking an experienced Clinical Sales Representative to join our team in Warsaw, PL. As a Clinical Sales Representative, you will be responsible for promoting our company's products and services to existing and potential clients in...

Job DescriptionAt TN Poland, we are seeking a highly skilled Clinical Research Professional to join our international team. As a Senior Clinical Trial Specialist, you will play a crucial role in providing feasibility services, contributing to business development, and ensuring the smooth conduct of newly awarded trials.This is an excellent opportunity for...

ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development. We're seeking a highly skilled Safety Scientist to join our diverse and dynamic team.As a Safety Scientist at ICON, you'll be responsible for designing and analyzing clinical trials, interpreting complex medical...

Are you an expert in graphic design looking to apply your skills in a fast-paced environment? Do you have a passion for creating visually appealing documents?We're seeking a highly skilled Clinical Trial Document Specialist to join our team at PSI CRO. As a specialist, you'll be responsible for designing and developing clinical trial documents that meet...

Job OverviewWe are seeking an experienced Clinical Research Associate to join our team at August Research. As a key member of our clinical research team, you will be responsible for site identification and selection, regulatory submissions, monitoring for clinical studies, and local safety reporting.This is a full-time position for candidates with at least...

About Clinical ResearchClinical research plays a vital role in advancing medical breakthroughs and bringing life-changing therapies to patients. At Care Access, we unite standard patient care with cutting-edge treatments and research, paving the way for newer and greater treatments to reach the world.The Role of Operational Compliance AssociateThis position...

Goldman Sachs is committed to delivering secure and resilient applications. Our Technology Risk team works tirelessly to identify and mitigate potential risks. As a member of this team, you will play a critical role in ensuring the security of our software development life cycle.We are seeking an experienced Application Security Expert to join our Secure...

Role OverviewThe R&D Procurement Manager in Clinical Services will be accountable for a category of outsourced services needed for GSK's clinical trials.This includes negotiating contracts with suppliers that secure favourable terms for procurement of goods and services contracts in line with the agreed business requirements.The successful candidate will...

Key ResponsibilitiesIndependently perform compliance checks, publishing, and finalizing various clinical and regulatory documents as per the checklist, SOP, and HTG. Ensure finalized/published documents are submission-ready and comply with GCP, HRA, and other applicable international standards.Prepare electronic compilations in accordance with functional and...

About the RoleThe Principal Medical Writer will be responsible for drafting, reviewing, and approving written assignments including marketing application submission documents. This role involves extensive clinical document expertise and supporting continuous improvement and best practices implementation.

The Medical Device Integration Expert role at TN Poland involves ensuring seamless integration of medical devices with existing systems for clinical trials.ResponsibilitiesDevelop and implement medical device integration solutions.Collaborate with cross-functional teams to ensure smooth integration.Analyze data to identify trends and areas for...

TN Poland is a leading provider of clinical research services, and we are looking for a highly skilled Audit Expert to join our team. As a Senior Quality Assurance Auditor, you will be responsible for conducting audits that impact business operations, processes, and systems.The Audit Expert will have extensive experience in quality assurance, regulatory...