Urgently required Clinical Officer at Ind Swift limited.
Qualification. M.Pharma(Preferably Pharmacology) Experience 3 to 5 years in Regulatory Companies.
1.knowlege of Bioequivalance study guidance for EU,AUS & USFDA for designing and protocol, finalisation.
2.writing/review of clinical study report writing.
3. Project Management of GCP and ICH guidelines.
4.literature search, review and preparation of clinical modules n non clinical modules for EU.
Please forward your CVs at hr.gbu@indswiftlabs.com or send it through whatsup at 8360051452.
