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4 results for Clinical Research jobs in Charleroi within a 30 km radius
Clinitude is a clinical research organization supporting pharmaceutical, biotech, medical device companies and site networks with our approach to complex trial data and regulatory submission challenges. * 1-3 years experience in direct sales, business development, or similar field , in clinical research * Research potential and obtain additional information on clients or on the needs of customer organizations. * Hands-on experience with clinical trial and pharmaceutical development preferred. * Basic understanding of CROs, and scientific and clinical data/ terminology, and the drug development process.
Clinitude is a clinical research organization supporting pharmaceutical, biotech, medical device companies and site networks with our approach to complex trial data and regulatory submission challenges. * 1-3 years experience in direct sales, business development, or similar field , in clinical research * Research potential and obtain additional information on clients or on the needs of customer organizations. * Hands-on experience with clinical trial and pharmaceutical development preferred. * Basic understanding of CROs, and scientific and clinical data/ terminology, and the drug development process.
No match yet? There are 3 more jobs that could match your search
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Ensure the Clinical Supply Quality activities are consistent across the range of different environments and teams supported (Vendors / / in house). * Proactively support the activities of Clinical supply for relevant manufacturing quality systems (deviation close out / Change management / complaints / quality improvement). * Support the of Clinical Supply Quality in ensuring an acceptable outcome of all audits and inspections, especially those by government agencies, as they pertain to Process Support and Package Development practices (where relevant), equipment, and facilities. * Ensure Clinical Supply Quality processes directly support Technical Operations and goals and objectives.
Ensure the Clinical Supply Quality activities are consistent across the range of different environments and teams supported (Vendors / / in house). * Proactively support the activities of Clinical supply for relevant manufacturing quality systems (deviation close out / Change management / complaints / quality improvement). * Support the of Clinical Supply Quality in ensuring an acceptable outcome of all audits and inspections, especially those by government agencies, as they pertain to Process Support and Package Development practices (where relevant), equipment, and facilities. * Ensure Clinical Supply Quality processes directly support Technical Operations and goals and objectives.
In-depth understanding of Health Authority compliance expectations for reporting quality-related issues (GMP, Clinical).
In-depth understanding of Health Authority compliance expectations for reporting quality-related issues (GMP, Clinical).
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In Belgium, we're at the forefront of basic technological and system research, product development, and market engageme nt.
In Belgium, we're at the forefront of basic technological and system research, product development, and market engageme nt.
7 exact matches jobs are outside your preferred location
Clinical Applications - Solution Area Specialist - Dutch Speaking
Clinical Applications - Solution Area Specialist - Dutch Speaking
Microsoft
Multiple Locations, Belgium
You will showcase the value proposition of Dragon Copilot in improving clinical documentation, provider efficiency, and patient outcomes. * You will serve as a knowledge leader in the role of AI-powered clinical documentation across diverse healthcare organizations, including hospitals, academic institutions, and large healthcare systems. * Proven experience delivering strategic presentations and communicating effectively across all levels of a healthcare organization including stakeholders such as Chief Medical Information Officers (CMIO), Chief Information Officers (CIO), Chief Nursing Officers (CNO), and departmental directors involved in clinical documentation and workflow optimization.
You will showcase the value proposition of Dragon Copilot in improving clinical documentation, provider efficiency, and patient outcomes. * You will serve as a knowledge leader in the role of AI-powered clinical documentation across diverse healthcare organizations, including hospitals, academic institutions, and large healthcare systems. * Proven experience delivering strategic presentations and communicating effectively across all levels of a healthcare organization including stakeholders such as Chief Medical Information Officers (CMIO), Chief Information Officers (CIO), Chief Nursing Officers (CNO), and departmental directors involved in clinical documentation and workflow optimization.
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Building a qualified pipeline across Europe (Pharma, Biotech, Clinical Trials, Diagnostics, 3PLs, High-Value Food)
Building a qualified pipeline across Europe (Pharma, Biotech, Clinical Trials, Diagnostics, 3PLs, High-Value Food)
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UZ Leuven * België - Solliciteer als één van de eersten - Introductie - Als grootste universitaire ziekenhuis van België wil UZ Leuven grenzen verleggen door gespecialiseerde zorg en innovatieve behandelingen te combineren met menselijke aandacht en respect voor elke persoon. Met meer dan 10.000 gepassioneerde medewerkers geven we elke dag de beste zorg op maat. We dagen onszelf uit en gaan voor kwaliteit op alle vlakken. Zelfs als het moeilijk wordt en bijna onmogelijk lijkt. We tillen elkaar naar een hoger niveau. Samenwerken zit in ons DNA. We zetten in op toonaangevend onderzoek en we geven opleiding aan jong talent. Onze beste ambassadeurs zijn de medewerkers van vandaag. Zij maken het verschil en verleggen grenzen, elke dag opnieuw. UZ Leuven wil mensen aantrekken met diezelfde drive en openheid van geest. Ben jij ook een grensverlegger? Verleg grenzen als kines
UZ Leuven * België - Solliciteer als één van de eersten - Introductie - Als grootste universitaire ziekenhuis van België wil UZ Leuven grenzen verleggen door gespecialiseerde zorg en innovatieve behandelingen te combineren met menselijke aandacht en respect voor elke persoon. Met meer dan 10.000 gepassioneerde medewerkers geven we elke dag de beste zorg op maat. We dagen onszelf uit en gaan voor kwaliteit op alle vlakken. Zelfs als het moeilijk wordt en bijna onmogelijk lijkt. We tillen elkaar naar een hoger niveau. Samenwerken zit in ons DNA. We zetten in op toonaangevend onderzoek en we geven opleiding aan jong talent. Onze beste ambassadeurs zijn de medewerkers van vandaag. Zij maken het verschil en verleggen grenzen, elke dag opnieuw. UZ Leuven wil mensen aantrekken met diezelfde drive en openheid van geest. Ben jij ook een grensverlegger? Verleg grenzen als kines
Conducting market research and commercial monitoring
Conducting market research and commercial monitoring
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Doelgerichte research en het testen van nieuwe software spreken je aan, en je weet dit nuttig te gebruiken bij je job.
Doelgerichte research en het testen van nieuwe software spreken je aan, en je weet dit nuttig te gebruiken bij je job.
As a Development Analyst, you will provide scientific expertise to contribute to manage physico-chemical method development activities for Biologicals Products from early clinical phases to commercial.
As a Development Analyst, you will provide scientific expertise to contribute to manage physico-chemical method development activities for Biologicals Products from early clinical phases to commercial.
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Research and identify potential customers within relevant industries, reaching out via cold calling, email, LinkedIn, networking events, and Suivo events.
Research and identify potential customers within relevant industries, reaching out via cold calling, email, LinkedIn, networking events, and Suivo events.
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Portfolio Monitoring and Reserving Analyst - Northern Europe
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Europ Assistance Belgium
Brussel
Partially remote
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