Regulatory Documents Jobs in Poland
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Senior Reg Publishing Specialist
Thermo Fisher Scientific
Work ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionSummarized Purpose:This is an outstanding opportunity to join Thermo Fisher Scientific as a Senior Reg Publishing Specialist. You will play a pivotal role in ensuring flawless regulatory review outcomes for key product achievements. Your...
Manager Medical Writing
Pfizer
Use Your Power for PurposeBy connecting evidence-based medical decision support with colleagues and stakeholders you will help achieve better health and treatment outcomes. Your work will ensure our evidence is scientifically robust provide unbiased and medically necessary expertise and investigate...
Regulatory & Start Up Specialist Ii, Iqvia Medtech...
Iqvia
Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Es...
Cmc Technical Writer
Gsk
At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples li...
Clinical Scientist, Hematology
Bristol Myers Squibb
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...
Site Coordinator
Psi Cro
The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.The function of the role may include but not limited to any/all of the following:Act as...
Business Process Analyst
Asstra
AsstrA is an international logistics company with over 30 years of experience. Our team of 1100 specialists operates in 23 countries across Europe Asia the USA and the CIS. We offer comprehensive transport solutions: road sea rail air and intermodal as well as customs clearance cargo insurance and p...
Regulatory Reporting Accountants
Kf
We are supporting a international organization in their search for a Regulatory Reporting Accountant to join their team in Warsaw. The organization is recognized for its commitment to operational excellence innovation and professional development. Their Warsaw office plays a strategic role in suppor...
Sas Programmer I, Ii, Or Iii
Baxter
This is whereyour work makes a difference.At Baxter we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater...
Site Coordinator
Psi Cro
The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.The function of the role may include but not limited to any/all of the following:Act as...
Artwork Implementation Manager
Pfizer
Job SummaryColleague fundamentally performs the ePALMS system Market Coordinator role in close collaboration with the Global Regulatory Sciences (GRS) Strategy functions at Pfizer Country Offices (PCOs) and is the central Regulatory point of contact for the PGS plants/Artwork Centers (AWC). Colleagu...
Principal Medical Writer
Gsk
Principal Medical WriterThe Principal Medical Writeris an individual expert contributor capable of independently executing complex writing assignments involving a thorough understanding of clinical trial designs and interpretation of statistically analyzed research data. He/she would be expected to...
Clinical Trial Site Coordinator
Psi Cro
Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.In this role you will:Act as the main line of communication between the Sponsor or CRO and the site.Ensure response to...