.../biotech environment (and/or relevant experience with a large CRO) in a clinical data management or closely related disciplineYou have a strong understanding of CDISC SDTMYou are able to organize and ...
...other consultantsABOUT YOU:You have a Master’s degree in life sciences, biotechnology, pharmaceuticals, or any relevant engineering fieldYou have between 2 and 5 years of experience within the pharmac...
...other consultantsABOUT YOU:You have a Master’s degree in life sciences, biotechnology, pharmaceuticals, or any relevant engineering fieldYou have at least a relevant internship or apprenticeship exper...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
.../technical study protocols and reports, and assess product impact from significant deviations.Compliance and Documentation: Ensure compliance with SOPs, global standards, regulations, and product regi...
...other enterprise equipmentAdministrate user access to systemsAssist other IT Team members in the implementation of major system changes, network redesign and system integrationsLog and document activi...
...other consultantsABOUT YOU:You have a Master’s degree in life sciences, biotechnology, pharmaceuticals, or any relevant engineering fieldYou have at least a relevant internship or apprenticeship exper...