Clinical Trial Medical Review Scientist

Site Name: WarsawPosted Date: Jan 23 2025Director, Medical Review Scientist (FTC)Fixed Term Contract 12 monthsGSK is expanding the Oncology Clinical Development organization and we are seeking experienced professionals to join our exciting journey. GSK Oncology has a commitment to the discovery and development of new oncology therapies with the life-changing...

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,...

**Job Description**GSK's Oncology Clinical Development organization is seeking an Associate Director, Medical Science Expert to join its Clinical Trial Medical Review Team (CTMRT). This role involves performing medical review activities across multiple oncology studies, ensuring the accuracy and completeness of clinical data.The ideal candidate will have a...

Job DescriptionThis role requires expertise in medical review, data interpretation, and clinical development processes. As a Director Medical Review Scientist, you will be responsible for ensuring the medical consistency and robustness of clinical data that cannot be processed by computerized means.The successful candidate will have experience using...

Our TeamGSK's Oncology Clinical Development team is a specialized group within the global Oncology Clinical Development function. We work seamlessly with fellow Oncology Clinical Development staff from a centralized work location, closely tied to other functions.The team is responsible for medical review activities across multiple oncology studies with...

Social network you want to login/join with:Clinical Medical Manager - Poland, WarsawClient:Location:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:98aeb9163027Job Views:2Posted:15.03.2025Expiry Date:29.04.2025Job Description:Are you looking for an opportunity where you can utilize your medical knowledge to communicate scientific...

4 days ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Company DescriptionPSI is a leading Contract Research Organization with more than 24 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services...

Clinical Trial Project CoordinatorWe are seeking a skilled Clinical Trial Project Coordinator to join our team at Thermo Fisher Scientific. As a key member of our clinical operations team, you will be responsible for providing technical support to project teams, coordinating non-clinical responsibilities, and ensuring the smooth execution of clinical...

Job DescriptionWe are seeking a skilled Freelance Regional Clinical Trial Coordinator to join our team at Rho, Inc. This is a home-based opportunity in Poland, Estonia, Lithuania, or Latvia.Main Responsibilities:Preparation of ISFs (Investigator Site Files) and maintenance of TMF (Trial Master File) or the CRO Project File.Communication and guidance to CRA...

Job DescriptionCare Access Research is seeking a highly skilled and experienced Medical Trial Coordinator Lead to oversee the day-to-day activities at our research site in Warsaw, Poland. As a key member of our team, you will be responsible for ensuring the successful execution of clinical trials, maintaining adherence to local regulations and Care Access...

OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...

About the OpportunityWe are seeking an accomplished Clinical Trials Writer to join our team at GlaxoSmithKline. This role involves developing clinical trial documents and managing projects to ensure timely delivery of high-quality documents.Key Responsibilities:Clinical Trial Document Development: Develop and review clinical trial documents, including...

OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...

Job Summary">The Medical Affairs Company (TMAC) is seeking a dynamic Oncology Clinical Advisor to join our client's innovative oncology team. This role offers an exciting opportunity to make a significant impact in the field of Head and Neck Cancer research and treatment.About the Role">Engage with Healthcare Professionals (HCPs) to provide high-level...

We are seeking a highly skilled Contract Analyst II to join our team!As a Contract Analyst II at ICON, you will be responsible for driving study initiation, maintaining effective communication with investigative sites and sponsors, and analysing contracts and agreements related to clinical trial activities.What You'll Do:Develop and execute plans for country...

Parexel International is seeking a Clinical Operations Assistant to support our Project Clinical Team.Responsibilities:Site Payments: Manage site payments, including processing invoices and tracking payments.Trial Master Files: Maintain accurate and up-to-date trial master files, ensuring compliance with regulations.Requirements:Qualifications: High school...

Job OverviewAt Comac Medical, we are seeking a skilled Clinical Research Associate to play a key role in the success of our clinical trials. As a Clinical Research Associate, you will be responsible for conducting feasibility studies and site qualification visits, developing strong relationships with investigators, and ensuring compliance with regulatory...

Social network you want to login/join with:Clinical Trial Manager - Poland - Infectious Disease, WarsawClient:MEDPACELocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:5f717e3db534Job Views:4Posted:28.03.2025Expiry Date:12.05.2025Job Description:OverviewMedpace is a full-service clinical contract research organization (CRO). We...

At J&J Family of Companies, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.We are seeking a Clinical Trial Operations Specialist to join our team in Warsaw, Poland. The ideal...

**Oncology Clinical Development Specialist**We are seeking an experienced Oncology Clinical Development Specialist to join our Clinical Trial Medical Review Team (CTMRT). This role involves performing medical review activities across multiple oncology studies, ensuring the accuracy and completeness of clinical data.The successful candidate will have a strong...