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Scientific Regulatory Candidates

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You’re looking for Scientific Regulatory experts . On BrightOwl, pharma, biotech and medical device experts (talent, candidates, …) register to view vacancies, and they built a profile (CV) in order for companies to find and contact them for new openings.

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100+ experts

Regulatory Affairs Associate

Courcelles, Belgium
Public Speaking Strategic Planning Microsoft Office Non-profits International Relations

Project manager in R&D during 9 years, I also benefit from 7 years of experience in administrative management.  Open for new opportunities, I followed a 9-months training in Regulatory Affairs a

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Company co-manager | RA scientific expert | Regulatory Affairs Associate | Project Manager | Project Manager
Interuniversity certificate Health Regulatory Affairs | FELASA level C animal experimentation | Ph.D. Biomedical Science ...
Gosselies, Charleroi, Belgium | Charleroi, Belgium | Louvain-la-Neuve, Ottignies-Louvain-la-Neuve, Belgium | Mons, Belgi ...

Clinical Data Manager/Statistical/Epidemiological Data Analyst, Regulatory Affairs, Medical/Scientific Writer

Belsele/Sint-Niklaas
Writing and review clinical regulatory documents Coducting surveys (quantitative and qualitative) Data management and analysis Scientific literature search Systematic review and meta-analysis

I am interested in positions in clinical research, epidemiology, data management and statistical data analysis but also in other domains of scientific research. I prefer a function with prospects, dev

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Researcher | Scientific Writer | Physiotherapist
Master's degree Epidemiology, clinical research and Research on health services, Master of Public Health (MPH) | Bachelo ...
Belsele/Sint-Niklaas

Regulatory Affairs Manager

Ghent, België
Regulatory affairs Life Sciences eCTD IND Clinical Development

Skilled Life Science professional with medical and scientific background.

Leading regulatory writer for EU & US submissions, experienced in (e)CTD and lifecycle management.

Specialised in regulato

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Associate Director Regulatory Affairs | Regulatory Affairs Manager | Senior Regulatory Affairs Associate | Medical Writer | M ...
Ghent University Hospital - Dpt. of Neurology | Master of Science (MSc) Biology
Ghent, België

Regulatory Affairs Manager

Rhône, France
Biotechnology Regulatory affairs Regulatory Requirements Global Regulatory Compliance Lifesciences

I am a goal oriented manager with extensive experience in global governmental, public, corporate and regulatory affairs management in several sectors (food, feed and biotechnology). My skills are base

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Regulatory Affairs Manager | Regulatory Affairs Specialist, Biotechnology | Project Manager, fresh produce imports | Project ...
PhD Phytopathology / Plant-Microbe Interaction | MSc Biology
Rhône, France | Brussels, Belgium

Regulatory Operations Manager

Mölndal, Västra Götland, Sweden
molecular biology Life Sciences Confocal Microscopy Electrophysiology Cell Culture

I am an experienced professional in Regulatory Affairs, Medical Writing, Research and Project Management. My career objective is to create a positive impact on society by ensuring development of Safe

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Regulatory Operations Manager | Global Labeling Proofreader/Regulatory Affairs Assistant | Consultant | PhD Student in Molecu ...
Masters in Medical Biosciences Human health and diseases; From cellular to clinical aspects | Bachelor of Technology (BT ...
Norway | Sweden | Denmark | Finland | Stockholm, Sweden

Director Non Clinical/Consultant non clinical regulatory/toxicology

Lyon, France
molecular biology Phase III Phase IV Phases of clinical development (phase I to IV) Position Paper

I am a senior regulatory pharmaco-toxicologist with extensive experience (20 + years) in both biotech and blue chip international pharmaceutical companies and working as a consultant. I have a proven

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Director: Non Clinical (Toxicology/Pharmacology) | Consultant non clinical regulatory services/toxicology | Head of Non Clini ...
Ph.D. Biological sciences | Bachelor of science Applied Biology | Nursing RGN
France | Switzerland | Belgium | Netherlands | Lyon, France

Regulatory and Quality Lead

Barcelona, Spain
Asuntos normativos Sistema de gestión de la calidad Gestión de proyectos Gestión y motivación de equipos Mejora continua

MSc Industrial Pharmacist by University of Barcelona with over 14 years of experience in the Pharmaceutical and Medical Device industry. Roles of increasing responsibility in Regulatory Affairs, Quali

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Quality & Regulatory Manager | Regulatory & Quality Lead Europe. | Regulatory & Quality Manager Iberia | Senior Regulatory Af ...
Master Pharmaceutical Sciences | Bachelor Pharmaceutical Sciences
Barcelona, Spain | London, UK | Zürich, Switzerland

Regulatory Affairs Specialist

Leuven, Belgium
molecular biology Cell Culture Immunology Cell biology Proteomics

I am an enthusiastic and eager-to-learn professional with experience in life sciences in both the academic and the biotech industry environments. I have a PhD in Biomedical Sciences and over 9 years e

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Regulatory Affairs CMC Specialist | Regulatory Affairs Expert Consultant | Wetenschappelijk medewerker | PhD student | Under ...
Doctor of Philosophy (PhD) Biomedical Sciences, General | Bachelor's degree Biological Sciences | Master's degree Medica ...
Leuven, Belgium

Regulatory Affairs Consultant/Medical Writer

Israel
FDA Life Sciences Regulatory affairs Technical Writing Medical Devices

I have a wide range of multi-disciplinary experience including: * Academic research in a hospital environment * Industrial experience in both agricultural and medical fields * Project management * Reg

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Independent Regulatory Consultant, Medical Writer and Technical Writer | Project Manager | Project Manager | Project Manager ...
Master of Science (MSc) Plant Pathology | Bachelor of Science (BSc) Biology | PhD Biology
Israel

Scientific Associate and Regulatory Affairs Manager Trainee

Belgium
Cell biology Biochemistry R&D Scientific writing 21 CFR Part 11

Multidisciplinary scientist with experience in biopharmaceutical insdustry (R&D and Analytical Approaches). Training in Regulatory Affairs, including Pre-and Post-Marketing Authorization Regulator

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Associate Scientist
Ph.D. Molecular Virolgy and Immunology | Diploma of Specialized Sutdies (D.E.S) in Biotechnologie Biochemistry and Biote ...
Belgium
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