Lead Clinical Document Writer

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...

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...

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...

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...

Job DescriptionThis position is a key role in the development and maintenance of data quality standards. The successful candidate will lead the implementation and maintenance of internal data quality control programs, acceptance criteria for data from external sources, and perform related programming tasks.The ideal candidate will collaborate with the...

B2B S.A is seeking a skilled Technical Writer to join its team. As a Technical Writer, you will be responsible for creating high-quality technical and operational documentation.This role requires excellent writing skills, as well as the ability to manage multiple stakeholders across different organizational levels.The ideal candidate will have a strong...

Job DescriptionWe are seeking a highly skilled Clinical Trial Lead to join our team at PSI CRO. As a Central Monitoring Manager, you will be responsible for leading the implementation of risk-based monitoring approaches on clinical study and program levels.You will:Facilitate initial and ongoing study Risk Management activities.Participate in the selection...

We are looking for an experienced Clinical Data Specialist Lead to join our Data Management team at GlaxoSmithKline. As a key member of the team, you will be responsible for providing DM operational input into study design, protocol, and study planning.The ideal candidate will have experience in clinical data management processes, standards, and systems, as...

Country Clinical Leadlokalizacja: Warszawa (mazowieckie)numer referencyjny: 1190881/jobs.plforma zatrudnienia: Pełny etatKey Responsibilities:• Act as the local representative of the company authorized by the Managing Director, to oversee legal affairs, human resource management, regulatory intelligence and compliance, financial management, vendor...

As a Document Production Manager at GSK, you will oversee the production of high-quality written content to support the company's mission.About the Role:This role involves working closely with cross-functional teams to develop and implement strategic plans for creating high-quality written content.Responsibilities:Drafts and reviews written content for...

The Senior Medical Writer position at GSK requires a unique blend of technical and interpersonal skills.About the Role:You will work closely with cross-functional teams to develop and implement strategic plans for creating high-quality written content.Responsibilities:Drafts and reviews written content for accuracy and quality.Coordinates the process to...

Key ResponsibilitiesAs a Medical Writer, you will be responsible for:Developing high-quality content for promotional and educational materials.Ensuring accuracy and consistency in all written materials.Collaborating with cross-functional teams to meet project deadlines.Providing scientific support for pitch research and development of complex...

About the RoleWe are currently hiring a Freelance Clinical Project Manager to work remotely on a freelance basis, managing international Phase I-IV clinical trials.The successful candidate will have excellent leadership and organizational skills, with a proven track record of delivering projects on time and within budget.Main ResponsibilitiesManage...

Oncology Clinical Development TeamWe are expanding our Oncology Clinical Development organization and seeking experienced professionals to join our team. As a Director, Medical Review Scientist, you will be responsible for performing medical review activities across multiple oncology studies.Key ResponsibilitiesMedical Review ActivitiesPerform medical review...

Our TeamWe are a dynamic and innovative team dedicated to delivering high-quality clinical systems and internal applications.We are seeking a talented Senior Software Engineer to join our team and contribute to our organization's growth and success.Responsibilities and Requirements:Work collaboratively with the IT team to design, develop, and implement...

About the RoleWe are seeking a highly skilled Senior Project Manager to lead our clinical trials in Poland. As a key member of our team, you will be responsible for ensuring the successful delivery of projects from start-up to closure.ResponsibilitiesServe as primary contact for sponsors and ensure timely updates on trial progressOversee project planning,...

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...

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...

Our Ideal CandidateWe are seeking an experienced and skilled Senior Medical Writer who can lead our team in delivering high-quality medical writing projects. The ideal candidate will have a strong background in medical writing, excellent communication skills, and the ability to work independently and collaboratively as part of a team.The successful candidate...

About UsRho, Inc. is a full-service Contract Research Organization (CRO) based in North America.We offer a comprehensive benefits package for all benefit-eligible employees and encourage a work-life balance that allows employees to bring their best selves to work.Job Title: Freelance Clinical Project ManagerMain ResponsibilitiesManage international clinical...