Clinical Writer Expert

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.

Medical WriterYour responsibilitiesAssist in the preparation of medical and scientific documents, including manuscripts, clinical study reports, abstracts, posters, and presentations. Conduct literature searches and analyze scientific data to support content development. Summarize clinical and scientific...

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...

Join us at Intecrowd as a Certified Financial or HCM Report Writer Consultant and become a part of our dynamic AMS Team. As an AMS Consultant, you will be responsible for providing functional and strategic support for our client's Workday technology.DutiesWorkday certification in Financials Core, Practical, or Advanced Reporting is required.As a subject...

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...

Clinical Application Specialist RoleWe are seeking a highly skilled Clinical Application Specialist to join our team in Healthcare Informatics.This role involves providing clinical user training, optimizing workflows, and ensuring the best use of advanced visualization and AI applications.As a key member of our Enterprise Informatics team, you will work...

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...

The role involves working closely with the Global Program Team to manage legal risk within development programs. Key responsibilities include providing pragmatic, solutions-oriented legal advice to colleagues across all levels of the organization. Additionally, the successful candidate will participate in Legal Department projects and initiatives, as well as...

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...

Job DescriptionWe're looking for a highly skilled Medical Writer to join our expert team at Publicis Le Pont. In this role, you'll be part of a group of writers overseeing quality content development, providing project and scientific counsel, and guiding both internal and external teams on current and new business projects.Your engagement will...

Job OverviewAt GlaxoSmithKline, we are seeking a highly skilled Principal Medical Writer to join our team. This role requires an individual with advanced regulatory medical writing experience and a thorough understanding of clinical trial designs and data interpretation.

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 RoleThis Senior Medical Writer position is a key opportunity to take on a leading role in preparing assigned documents, including confirming scope, templates, and specifications. Strong communication skills are essential for negotiating timelines and discussing customer comments.The ideal candidate will have excellent written and oral communication...

We are a global company dedicated to improving medical science and bringing new medicines to those who need them.About the JobThe Clinical Data Scientist is a key member of our team, working with clinical trials patient and operational data, developing new data solutions, and setting up Risk-based Monitoring systems in the Process Improvement...

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...

About the RoleTN Poland is seeking a highly skilled and experienced Clinical Project Manager to lead challenging full-service global clinical research projects.The ideal candidate will have recent clinical research experience in project management and a strong therapeutic background in oncology, MS, IBD, hemophilia, rare disease, or infectious diseases.Key...

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...

Compliance ExpertWe are seeking an experienced Compliance Expert to join our Quality Assurance team in Warsaw, Poland. As a key member of the team, you will be responsible for ensuring compliance with regulations, guidelines, and operating procedures through independent clinical audits.Key Responsibilities:Conduct independent clinical audits to assess...