Société : CK Group Lieu : Beerse Flanders Site source : Talent BE
In concert with operational staff, acts as a liaison between the company and clinical investigators for overarching scientific guidance and other potential non-medical aspects.
Be responsible for the TA review and sign off on various operational plans.
Be Responsible for scientific input into HA and EC responses.
Lead data visualization (DV) meetings and ensures decisions are documented and communicated internally and externally.
Qualified CS may perform aspects of medical review under supervision of CL or SRP.
Requirements:
Right to work in the EU is essential.
PhD in relevant field (neuro, biology, chem, pharmacy,) PharmD or MD degree.
Experience in clinical research/drug development that has exposed the individual to the rigors of human trial conduct with pharmaceuticals, devices, basic clinical practice with the precepts of Good Clinical Practice.
Apply:
Right to work in the EU is essential.
Please quote job reference T56732 in all correspondence. CK Group BeerseFlanders
