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Regulatory And Start Up Specialist Candidates

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You’re looking for Regulatory And Start Up Specialist 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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9 experts
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Research Assistant

Helsinki, Finland
Customer Service PCR Agarose Gel Electrophoresis Biomaterials Biomedical Engineering

• Researcher in Virology group, University of Tampere (asthma, rhinoviruses, hygiene hypothesis, RT-qPCR)

• Customer service experience from >10 years

• Interested in event organizing and net

Scientific Researcher | Registration and info desk worker | Master's Thesis Student in Virology Group | Manager of ticket ins ...
Master of Science (M.Sc.) Biotechnology, Specialization in Cell and Tissue Technology. | Minor in Chemistry Biotechnolog ...
Helsinki, Finland | Espoo, Finland | Helsinki, Finland

Regulatory Affairs Associate

Charleroi, Belgium
GC-FID GC-MS IR spectroscopy GPC Analytical Chemistry

Working in a CRO I am the clinical regulatory affairs referent for European projects. I have a sound experience dealing with Clinical Trial Applications (CTA) both to competent authorities (CA) and et

Regulatory Affairs Consultant | Senior Analytical Chemist | Analytical Chemist | Trainee Analytical Chemist, Eurodyssée prog ...
Clinical Research | Master of Science (MSc) Chemistry | Research Project Analytical Chemistry
Charleroi, Belgium


Rotterdam, Netherlands
pharmacology Pharmaceutics Chemistry Analytical Chemistry Organic Chemistry
Freelance Reviewer and Proofreader (English to Italian/Pharmaceutical and Biotechnological patents) | Volunteer translation w ...
5 years course equivalent to BSc and MSc Pharmaceutical Chemistry and Technology
Antwerp, Belgium | Brussels, Belgium | Italy | UK | Netherlands

Senior Clinical Research Associate

Prato, PO, Italia
Clinical research Clinical monitoring Clinical Study Design CMC Regulatory Affairs Contract negotiation

Free-lance with over 25 years of experience in medical dept of pharmaceutical industries and global/national CROs

degree Pharmaceutica chemistry
Prato, PO, Italia

Clinical Trial Consultant (Clinical PM/Reg PM/SSU)

Clinical Research Consultancy EMEA Region Clinical trials Vaccines Regulatory submissions
Freelance Contractor Senior Regulatory Project Manager | Freelance Contractor Senior CRA | Executive Director and Senior Cons ...
Master in Chemistry Clinical Research | 8u Mathematics

Business Consultant

Amsterdam, Netherlands
KOL management Starting up local Biotech Reimbursement strategy oncology Hematology

Creating entrance in new markets, building strong indepth KOL relationships, cross functional leading skills. Startup of Investigational Initiated Trials (IIT’s or IST's) Broad network in Dutch and B

Medical Science Liaison | Market Access Manager BNLX | Business Consultant / Executive Partner | Consultancy services for US ...
Postdoc Management | MSc Biomedical Sciences | Propaedeuse Chemistry
Belgium | Netherlands | Amsterdam, Netherlands

Regulatory Affairs Manager

Leuven, Belgium

Professional Objective: Looking for a Regulatory affairs position in CMC

After an education in biochemistry and chemistry, I hold a PhD degree in biotechnology. I gained relevant and various academic

Regulatory Affairs Manager | Scientific Assessor | Regulatory & Project Specialist | R&D Scientist in Industrial Biot ...

Manager Business Development

Düsseldorf, Germany
Clinical Site Monitoring Phase I Clinical trials ICH-GCP Proof of concept

•      Clinical Research Professional with 9 years' experience in clinical development in pharmaceutical/biotech industry, CROs and academia
•      Expertise area in early clinical developm

Manager Business Development | Jr. Early Stage Development Scientist /Sr. CRA | Clinical Research Associate (CRA) | Clinica ...
Doctor of Medicine (M.D.) Medicine | Specialist Functional and Ultrasound Diagnostics | General Practitioner Therapy
UK | Belgium | Netherlands | Germany | France

QA Manager, Lead Auditor

Île-de-France, France
Quality Assurance Good Clinical Practice (GCP) GCLP ISO 15189 Good Laboratory Practice (GLP)

R&D Quality Assurance Professional, Clinical Trials Auditor, Root Cause mapping specialist and Risk-based thinker, always interested by QA leadership and/or Auditing opportunities in Europe or Nort

Consultant, Project Manager | Clinical QA Consultant | QA Manager | Scientific consultant | PhD student
PhD Molecular Genetics & Genomics | Master Infectious disease & Vaccinology
Lyon, France
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