is Hiring For Pharmacovigilance @ Pune Location

Greetings from WiproWe are hiring for Pharmacovigilance Case processer @ Pune locationExperience- 1- 2 yearsQualification- B. Pharm/ M. Pharm with valid Pharma licenseOnly the qualifications mentioned are eligibleCandidate should have excellent Communication in EnglishShould be ready for Rotational shiftsShould have excellent knowledge of...

As a Pharmacovigilance Associate you are part of the Pharmacovigilance Department (sometimes called the Drug Safety Department). Your role is one of reporting adverse effects (AEs) and side effects, in accordance with the current Dutch and European legislation for pharmacovigilance. You may also train colleagues in departments such as marketing and sales,...

Pharmacovigilance is the most precise way for evaluation of the relevancy of Clinical Research. In this the tests are conducted under observation whether a new innovative product performs as expected or not. There is ‘n’ number of innovative therapies generated in laboratories but very few of them survive & reach to the point of human testing. It...

My profile :- SALESFORCE DEVELOPER With PHARMACOVIGILANCE Job Title: Salesforce Developer Payroll of :- Client name - Qbranix Exp level - 4 to 7 years Location : Pune Resource Type: Contract Type of work: 6 month initially and extended based on the project Start Date: Immediate - PF Mandatory Budget - 15 LPA Mandatory Qualifications: Experience...

My profile :- SALESFORCE DEVELOPER With PHARMACOVIGILANCEJob Title: Salesforce DeveloperPayroll of :- Client name - QbranixExp level - 4 to 7 yearsLocation : PuneResource Type: ContractType of work: 6 month initially and extended based on the projectStart Date: Immediate - PF MandatoryBudget - 15 LPAMandatory Qualifications:Experience Pharmacovigilance (PV)...

As a Pharmacovigilance Associate you are part of the Pharmacovigilance Department (sometimes called the Drug Safety Department). Your role is one of reporting adverse effects (AEs) and side effects, in accordance with the current Dutch and European legislation for pharmacovigilance. You may also train colleagues in departments such as marketing and sales,...

**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...

1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. - Ensure appropriate interpretation...

**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...

Division Research and Development / Global Drug Development / Worldwide Patient Safety/Medical Safety Assessment (MSA) Functional Area Description The Worldwide Patient Safety group is responsible for ensuring the safety of our medicines: The Worldwide Patient Safety group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including...