Zoekresultaten: 89 vacatures
...Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director
Positions in GSK Safety Evaluation and Risk Management (SERM... ...clinical matrix.
~ Leads the safety component of global regulatory submissions.
~ Expert evaluation skills and analytical thinking...
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...ensured in Belgium, Luxembourg, and the Netherlands
The Regulatory function values both working together as a team and independently... ...good relationships with internal (Global Regulatory Leads, Pharmacovigilance, Business partners, Market Planners, …) and external...
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...Regulatory Affairs Specialist page is loaded Regulatory Affairs Specialist
Apply locations Brussels area, Belgium posted on Posted 27 Days Ago job requisition id 2024-12893 About the Role
Become part of the Legal & Compliance team
The Legal & Compliance team...
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Job summary
An exciting opportunity has arisen to recruit a full time Administrator to support the Quality Regulation and Improvement Department based at London Ambulance Service's Headquarters. This is a full time and permanent position.
We are looking for an experienced...
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...For our Diabetes Care division, we are recruiting a Senior Regulatory Specialist for Benelux.
The Senior Regulatory Specialist is responsible for managing an efficient program to ensure that all regulatory activities for Abbott Diabetes Care products are achieved to...
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...When our values align, there's no limit to what we can achieve.
We are seeking an experienced Regulatory Affairs Consultant to join our team. As a Regulatory Affairs Consultant, you will be responsible for providing expertise in registration Regulatory Affairs, with...
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...Belgium, or Raleigh, North Carolina, US, or UK, we are looking for a talented individual to fill the position of IT Solution Expert Regulatory & Quality
About The Role
This role has global responsibility for all IT systems that enable the Regulatory and Quality...
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...us get ahead of disease together with our Internship Programme
Education required: You are regularly enrolled in a Master in Regulatory Affairs, Engineering, Pharmacy, Biology, Chemistry, Bio-engineering or similar field in an Educational Establishment located in...
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Stage
...When our values align, there's no limit to what we can achieve.
Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This...
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Thuiswerk
...- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical...
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...- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical...
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Stage
...- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical...
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Stage
...arena.
b) The management and control of all label content regulatory requirements and translations within the SMART LS label... ...services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support...
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...resolution of issues involving a range of technical, quality, regulatory and operational issues to ensure patient supply without... ...services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support...
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Stage
...- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical...
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Stage
Director, Senior Director & Executive Director, Safety Physician SERM (Safety Evaluation & Risk Mana
...with appropriate PV experience), with additional relevant medical or scientific post-graduate qualifications.
Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities...
...the budget for the operations department and ensure that all expenses are within budget.
Ensure compliance with all relevant regulatory requirements.
Required competencies
You have (required) :
Bachelor's degree in Business Administration, Engineering, or...
Met contract
...procedures and scientific reports. Significant contribution (autonomous writing and review by N+1) to and direct interactions with the Regulatory/IP teams for the preparation of the preclinical section of Regulatory/IP documents, in own area of technical expertise...
...outside of IT.
Proficiency in reporting and data analysis, particularly with PowerBI.
Nice-to-Have Criteria:
Experience in a regulatory environment.
Previous role as a Solution Architect within the Office 365 domain.
Candidates should possess a blend of...
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30 € per uur
...recommended processes and new technologies to the benefit of the process activities, of the MU and the whole organization.
Quality / Regulatory:
~ Ensure adherence of the technical services to legal constraints, local and international standards, cMP, Regulatory...
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