- Planet Pharma
- Oost-Vlaanderen
- 1 week geleden
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...scientific and methodological expertise for study protocols, data analysis plans, and publicationsAssess and recommend external data sources such as disease registries, claims databases, and EHRsContr...
- Planet Pharma
- Antwerpen
- 1 week geleden
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...scientific and methodological expertise for study protocols, data analysis plans, and publicationsAssess and recommend external data sources such as disease registries, claims databases, and EHRsContr...
- Planet Pharma
- Brussel
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...scientific and methodological expertise for study protocols, data analysis plans, and publicationsAssess and recommend external data sources such as disease registries, claims databases, and EHRsContr...
- CONSULTYS BENELUX
- Henegouwen
- 1 week geleden
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- West-Vlaanderen
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- West-Vlaanderen
- 1 week geleden
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- Antwerpen
- 1 week geleden
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- West-Vlaanderen
- 1 week geleden
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- Henegouwen
- 1 week geleden
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- West-Vlaanderen
- 1 week geleden
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- Antwerpen
- 1 week geleden
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- Brussel
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- Luxemburg
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...scientific/technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and pr...
- CONSULTYS BENELUX
- Brussel
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Consultys BENELUX is looking for a Life Science Consultant to join its consulting team in VIE.As Life Science consultant, you will support our clients on diverse projects related to QA, QC, C&Q, CSV, ...
- Planet Pharma
- Brussel
- 1 week geleden
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...Scientific Literature Management platform by gathering and analyzing user requirements, preparing and distributing an RFI, evaluating vendor responses, and helping to create a detailed RFP. This role ...