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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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8 experts
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Clinical research Clinical trials Lifesciences Clinical Development Medical writing

Three years experience in Cinical Trial management in Romania, study monitoring, quality assurance, biostatistics, site management, SOP editing, writing, regulatory affairs. More than 7 years experien

Associate of Professor | Study Physician | Internal Medicine Specialist (physician) - Investigator | Partner | CEO
Doctor of Philosophy (Ph.D.) Internal Medicine

Preclinical Research Manager

Nivelles, Belgium
Immunology Infectious diseases Vaccines Immunomodulation Project Management

My PhD in Biomedical Sciences followed by 6 years of postdoc experiences in academia and pharma industry allows me to acquire strong expertise in immunology. I have demonstrated during my last experie

Expert Scientist - Vaccine Research, R&D | Postdoctoral Research Scientist - Vaccine Research, R&D | Postdoctoral Res ...
Doctor of Philosophy (Ph.D.) Biomedical Sciences
Nivelles, Belgium

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

IT Manager

Wavre, Belgium
Business Analysis Business Intelligence Financial Analysis Performance Management Internal Controls
IT Manager | Managing Director | Business Analyst Solvency II | Business Architect | SOXli Team leader
MBA Economics
Walloon Brabant, Belgium | Wavre, Belgium

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

Project Specialist

Milan, Italy
Project Management Translation Italian GCP Clinical research

8 years of relevant operational experience in a leading global bio/pharmaceutical services organization. Experienced in international full service, phase II , III and PACE global studies across several

Sr. Project Specialist | Project Assistant | Interpreter | Customer service and airline booking agent
Regional Rescuer Certification 118 Medical emergency | Italian | English and Psychology | English | Associate Event o ...
Milan, Italy

Lifesciences Consultant

Vilvoorde, Belgium
Biotechnology Pharmaceutical Industry Lifesciences oncology Immunology
Engineering, Project Management | Owner, Division Market Access, HealthEconomics and Regulatory Affairs | Owner BioDataPharma ...
Doctor of Medicine (MD) Medicine | Health Economics | Business Engineering | Certificate in Stress and Burn-out Manage ...
Vilvoorde, Belgium

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 ...
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