Clinical Publishing Expert

Job Overview:Regulatory Affairs Senior PositionWe are looking for a seasoned Regulatory Affairs Senior to join our team at Randstad Polska Sp. z o.o. This is a unique opportunity for a professional with a strong background in regulatory affairs and submission publishing.The successful candidate will have extensive experience with various submission and...

We are looking for a highly skilled Submissions Publishing Expert to join our team at ManpowerGroup Sp. z o.o.About the RoleThis position involves working on the execution of electronic publishing of moderate to complex regulatory submissions for national, regional, and global regulatory agencies and operating companies in both eCTD and non-eCTD format.Main...

Job OverviewWe are a technology-led healthcare solutions provider driven by our purpose to enable healthcare organizations to be future-ready.This role involves performing technical quality checks and ensuring procedural compliance as per electronic submission requirements and internal SOPs, standards, and executing publishing, uploading to EDMS (Veeva),...

At ManpowerGroup Sp. z o.o., we are a global leader in the employment industry, operating in 82 countries and serving clients across various industries.Job OverviewWe are seeking a Regulatory Affairs Publishing Specialist to join our team, who will be responsible for executing electronic publishing of regulatory submissions for national, regional, and global...

Key Responsibilities:The ideal candidate will utilize regulatory information management systems and tools to assemble, publish, validate, dispatch, and archive complex submissions according to internal processes and regulatory guidelines. They will also proactively interact and support RA and cross-functional partners for submission-related needs and issues,...

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 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...

This Regulatory Affairs Publishing Specialist role offers an exciting opportunity to work with a global team and contribute to innovative projects.The successful candidate will be responsible for executing the electronic publishing of moderate to complex regulatory submissions for national, regional, and global regulatory agencies and operating companies in...

Job OverviewWe are seeking a highly skilled Clinical Country and Site Lead to join our team at Biogen. This role will be responsible for providing strategic direction and oversight for clinical trials in Poland.The ideal candidate will have extensive experience in managing clinical trial activities, including sponsor oversight activities in an outsourced...

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 Trials ExpertWe are looking for an experienced Clinical Trials Project Manager to join our team. As a seasoned professional, you will be responsible for managing clinical trials from start to finish, ensuring compliance with regulatory requirements and meeting client expectations.ResponsibilitiesDevelop and manage clinical trial protocols, informed...

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...

Required Skills and QualificationsBachelor's Degree/Master's Degree in Science (Pharmacy, Life Science).Technical Knowledge: MS Word, PDF, Veeva, ISITool Box.4-7 Years of experience in the clinical publishing domain and experience with preparing clinical submission documents in submission-ready format.

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...

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...