Clinical Trials Jobs in Budapest
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Clinical Trials Assistant 1
Qet Iqvia Rds Egypt
Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) tea...
Medical Science Liaison
Astrazeneca
Medical Science Liaison (Oncology Breast Cancer)ResponsibilitiesProvidescientific and medical supportwithin the assignedtherapeutic area aligned with the relevantcross-functional strategyandmedical plan.Leadongoing non-promotional scientific exchangewithkey external experts strengthening existing r...
Medical Lead Big Pharma Oncho-hematology Budapest
Carbyne
On behalf of a Global Top Big Pharma client we are currently seeking an experienced Medical Affairs professional for a Medical Lead this role the successful candidate will lead a small team and take overall responsibility for the Medical Affairs activities within the companys Onco-Hematology therap...
Iot Global Regulatory Affairs Manager (ref5219a)
Deutsche Telekom It Solutions
Ihre Aufgaben: In dieser Position sind Sie verantwortlich für die kontinuierliche Analyse und Bewertung der regulatorischen und marktlichen Rahmenbedingungen der Länder in die die Deutsche Telekom IoT Connectivity und Connectivity-nahe Produkte verkauft bzw. aus diesen Ländern bezieht. Sie beraten I...
Clinical Research Associate I Fso
Fortrea
WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.You will be responsible for (but not only):All aspects of study site monitor...
Medical Advisor Oncology
Abbvie
Develop and maintain in-depth knowledge of the designated product (s) and therapeutic areas (TAs) including through participation in internal discussions trainings relevant congresses and seminars and regular independent study of publications literature and guidelines.Providing scientific expert adv...
Senior Site Manager
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Clinical Trial Assistant Hungary Based
Iqvia
IQVIA is looking to hire a motivated Clinical Trial Assistant Single Sponsor Dedicated HungaryJob Overview:CTA performs daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery....
Supplier Relationship Specialist I
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...
Dir Global Site & Study Operations
Amgen
Career CategoryClinicalJob DescriptionAccountabilitiesThe Country Study and Site Operations Head is accountable to drive all country and hub & spoke execution and quality measures including study operations site operations and site engagement while ensuring operational capabilities support the deliv...
Junior Legal Counsel
Psi Cro
If you are an enthusiastic legal professional you may be the expert we are looking for to join our dynamic team. As a Junior Legal Counsel you will review and negotiate contracts in close cooperation with the project teams and provide legal advice on employment data protection and other corporate ma...
Clinical Research Associate Ii
Psi Cro
As a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.This is a hybrid role in the Budapest Hungary office.You will:Conduct and report SIV RMV...
Procurement Specialist Iii – Lab Category
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...
Lead Supplier Relationship Manager
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...
Site Budgeting And Contracting Specialist Client D...
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin us as a Site Contract Specialist Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 count...
Clinical Scientist Oncology-hematology Cns Immunol...
Iqvia
Job OverviewThe Clinical Scientist supports medical monitoring and scientific tasks on projects under theguidance of Therapeutic Medical Advisors (TMA) and in collaboration with the crossfunctional project team. These activities enable the use of high quality scientific data to make timely decisions...
Site Budget & Contract Specialist 24 Months Fixed ...
Fortrea
Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confidentiality agreem...
Medical Manager Oncology
Abbvie
Lead and develop the team of medical advisors/ MSLs/ Clinical scientific managers. Be the primary knowledge expert for assigned product(s)/ TAs through attendance/ participation at key internal meetings/ training sessions relevant congresses and seminars and by regular self-study of the publications...
Regulatory Submissions Associate Manager I Emea
Fortrea
Summary of Responsibilities:Coordinates and oversees Regulatory Authority Ethics Committee/Institutional Review Board Third Body submissions for all study types across multiple countries globally including EU CTR through CTIS platform.Develops submission strategies timelines and progress updates in...
Senior Statistical Programmer (fsp) Hungary
Parexel
When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...