Salesforce Developer With Pharmacovigilance

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)...

**Job Summary** Join our dynamic team as a Pharmacovigilance Specialist where you will leverage your expertise in Generative AI to enhance drug safety processes. With a focus on innovation and precision you will contribute to the development of safer pharmaceutical products. This hybrid role offers a unique opportunity to work in a collaborative environment...

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...

The Project Manager, Pharmacovigilance (PV) Solutions is responsible for day-to-day project management and oversight of non-linguistic PV projects, and may be in daily and regular contact with clients. This role is required to meet all client timelines and work in conjunction with fellow Project Managers, Project Coordinators, Python Specialists,...

The Project Manager, Pharmacovigilance (PV) Solutions is responsible for day-to-day project management andoversight of non-linguistic PV projects, and may be in daily and regular contact with clients. This role is required tomeet all client timelines and work in conjunction with fellow Project Managers, Project Coordinators, PythonSpecialists,...

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...

Processing adverse events reports from post marketing sources into Teva's global safety database: - The different sources / types of reports includes: Reports from the scientific literature, Teva partners (other pharmaceutical companies), Health Authorities, Non-interventional studies and other programs - The processing includes Adverse Events coding (in...

**Description** - Responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy, and execution of certain post-marketing commitments and ensuring compliance with global regulatory requirements. -...

**Job description** - Responsible for review of investigational new drug safety reports (INDSR) and submission to FDA (as applicable) - Responsible for negotiation and implementation of pharmacovigilance agreements (PVA) with business partners - Supports PV Clinical Specialists in tasks and projects as needed - Responsible for identifying and developing...

Company Description We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory...