Résultats de recherche

LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec CanadaContract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years’ experience working within Clinical Research within a CRO.This person should have expertise in LIMS, and SampleManagem

Watson LIMS Optimization Specialist – (Full-time) – Onsite – Quebec CanadaContract Research Organization seeks a full-time onsite Watson LIMS Optimization Specialist.Ideal candidate will have 2+ years’ experience in Watson LIMS having worked within an FDA, GLP, GCP and TPD regulated environm

LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec CanadaContract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years’ experience working within Clinical Research within a CRO.This person should have expertise in LIMS, and SampleManagem

Watson LIMS Optimization Specialist – (Full-time) – Onsite – Quebec CanadaContract Research Organization seeks a full-time onsite Watson LIMS Optimization Specialist.Ideal candidate will have 2+ years’ experience in Watson LIMS having worked within an FDA, GLP, GCP and TPD regulated environm

LIMS Clinical Studies Specialist (Full-time) Onsite Quebec Canada.Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years experience working within Clinical Research within a CRO.This person should have expertise in LIMS, and SampleManagement, Ligand

Watson LIMS Optimization Specialist (Full-time) Onsite Quebec Canada.Contract Research Organization seeks a full-time onsite Watson LIMS Optimization Specialist.Ideal candidate will have 2+ years experience in Watson LIMS having worked within an FDA, GLP, GCP and TPD regulated environment prior.A

Watson LIMS Optimization Specialist – (Full-time) – Onsite – Quebec Canada.Contract Research Organization seeks a full-time onsite Watson LIMS Optimization Specialist.Ideal candidate will have 2+ years’ experience in Watson LIMS having worked within an FDA, GLP, GCP and TPD regulated environ

LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec Canada.Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years’ experience working within Clinical Research within a CRO.This person should have expertise in LIMS, and SampleManage

Watson LIMS Optimization Specialist – (Full-time) – Onsite – Quebec Canada.Contract Research Organization seeks a full-time onsite Watson LIMS Optimization Specialist.Ideal candidate will have 2+ years’ experience in Watson LIMS having worked within an FDA, GLP, GCP and TPD regulated environ

LIMS Logistics Specialist – (Full-time) – Onsite – Quebec Canada.Contract Research Organization seeks a full-time onsite LIMS Logistics Specialist with 2+ years’ experience working within Clinical Research within a CRO.This person should have expertise in LIMS, and SampleManagement, Ligand B