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| Job Location | Gurugram |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Recruitment Services |
| Functional Area | Sales / BD |
| EmploymentType | Full-time |
Roles and ResponsibilitiesPrepare ACTD and CTD regional dossiersPreparation and review of dossiers as per the current prescribe guidelines of respectiveregulatory authorities.Preparation of registration and renewal dossiers.(BMR/MFR/PV/AMV) required for dossier.Desired Candidate Profileclinical trials/PSUR & TOXICITY studies.Analytical skillsStrong communication skills, both verbal and writtenSatish Kohli7895263093capitalplacement02@gmail.comPerks and BenefitsSalary: Not Disclosed by RecruiterIndustry: Medical / Healthcare / Hospitals Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology Role Category: Drug Regulatory Affairs/DocumentationRole: Regulatory Affairs ManagerEmployment Type: Full Time, Permanent , PG - Post Graduation Not RequiredDoctorate - Doctorate Not Required
Keyskills :
regulatory affairsanalytical skillspreparationanalyticalregistrationhospitalsregulatorystrong communication skillscommunication skillsfilingenvironmental toxicologyhealthcarecommunicationbiotechnologyctdbasisapicompilationmedical