Clinical Trials Writer

About Advanced ClinicalWe specialize in providing high-quality data solutions for clinical trials. Our team of experts is dedicated to delivering accurate and reliable data to support informed decision-making.What We OfferA dynamic and supportive work environment.The opportunity to work on challenging projects and develop new skills.A competitive...

About the RoleWe are seeking a highly skilled Senior Medical Writer to join our team. As a Senior Medical Writer, you will be responsible for creating high-quality written content for clinical trials and regulatory documents.Key Responsibilities:Create a range of clinical documents, including protocols, clinical study reports, NDA/MAA CTD submission...

About UsWe are a global biopharma company, GlaxoSmithKline, with a mission to unite science, technology, and talent to get ahead of disease together.We are seeking a highly skilled Clinical Writer Lead to join our team as a Principal Medical Writer.Job DescriptionDevelop high-quality clinical regulatory documents, including protocols, clinical study reports,...

Job Summary">We are seeking an experienced Medical Writer - Clinical Documents to join our team at GSK. As a key member of our content development group, you will be responsible for creating high-quality, regulatory-compliant medical content for clinical trials and submissions.Key Responsibilities:">Write and edit complex medical content, including...

We are seeking a highly skilled and motivated individual to join our team as a Clinical Trials Coordinator in Warsaw, Poland. As a Clinical Trials Coordinator, you will be responsible for providing administrative and logistical support to Clinical Trial Assistants, Site Managers, and Local Trial Managers in tracking progress of trials, managing study data,...

Research Coordinator - Clinical TrialsWe are seeking a highly skilled Research Coordinator - Clinical Trials to join our team at Thermo Fisher Scientific. In this role, you will be responsible for providing technical support to our clinical research team, ensuring the smooth execution of clinical trials.About the Position:This is a client-dedicated position,...

Drive groundbreaking medical research forward as a Clinical Research Coordinator with Hobson Prior International Ltd.This part-time freelance role in Warsaw requires an experienced professional to coordinate clinical studies at research sites, ensuring smooth operations and data management within clinical trials.The successful candidate will have a strong...

Clinical Trials Support SpecialistWe are looking for a skilled Clinical Trials Support Specialist to support the clinical development of Alexion's pipeline at early phases of development.Main ObjectivesDevelop and maintain the highest scientific and medical expertise in the relevant fields.Closely collaborate with cross-functional teams to support clinical...

Why Choose This Role?This Senior Medical Writer position at GlaxoSmithKline presents an opportunity to join a leading global healthcare company and contribute to delivering high-quality clinical documents.Key ResponsibilitiesDeveloping and implementing strategies for creating clinical documents that meet the organization's standards.Collaborating with...

Job SummaryWe are seeking an experienced clinical research professional to join our team as a Remote Clinical Trials Manager.In this role, you will be responsible for managing clinical trials from start-up to close-out, ensuring compliance with regulatory requirements and study protocols.As a key member of our operations team, you will collaborate with...

**About the Opportunity**We are seeking an experienced professional to join our team as a Clinical Trials Planning Specialist.The successful candidate will play a crucial role in operational strategy and planning within the pre-award space.The Clinical Trials Planning Specialist will be responsible for developing, analyzing, interpreting, and presenting...

Role SummaryThe Clinical Trials Support Professional role is responsible for supporting the collection, documentation, and reporting of safety data related to medications and clinical trials. This role requires strong organizational skills, attention to detail, and effective communication and collaboration skills.Key Responsibilities:Support the collection,...

IQVIA Argentina is seeking a Clinical Study Report Writer to join our team. As a Clinical Study Report Writer, you will be responsible for taking a leading role in preparing assigned documents, including confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, and...

Brief DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.Essential Functions/ResponsibilitiesProgram simple to complex data review listings, exception reports,...

Company Overview:We are a global healthcare company dedicated to accelerating medical innovation by making clinical trials more accessible and patient-friendly.Our mission is to bridge the gap between patients and doctors, ensuring seamless communication and timely access to life-changing treatments.Your Role:As a Clinical Trials Coordinator, you will be...

About GSK">GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies.">Job Summary">We are seeking a highly...

Job DescriptionThe Clinical Data Scientist plays an integral part of our team here at Psi CRO Ag. This role involves working with clinical trials patient and operational data, developing new data solutions, and setting up Risk-based Monitoring systems in the Process Improvement department.Hybrid work in Warsaw allows for a great balance between work and...

Job SummaryAs a Clinical Research Associate at Comac Medical, you will play a crucial role in ensuring the success of our clinical trials. We are seeking an experienced professional to join our team as a Site Operations Manager, responsible for overseeing the day-to-day activities of our sites. **Key Responsibilities:**- Conduct site qualification visits and...

Our Company OverviewMedpace is a leading global clinical contract research organization (CRO). We offer a comprehensive range of services, from Phase I to Phase IV clinical trials, to support the development of innovative medical treatments.About UsWe have a long history of successfully delivering projects on time and within budget. Our expert team provides...

Administrative Assistant Clinical Trials Role SummaryWe are seeking an experienced Administrative Assistant to support our Clinical Trials team. The successful candidate will provide high-quality administrative support, maintaining the highest level of professionalism and discretion.ResponsibilitiesAdministrative Tasks: Providing administrative support to...