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)...

A pharmacovigilance associate ensures compliance with applicable regulations or standard operating procedures; specialises in drug safety management, clinical trials and medical supervision. - Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and...

Job Title: Pharmacovigilance Team LeadAs a key member of our organization, you will play a vital role in overseeing the pharmacovigilance team and ensuring the highest standards of quality and compliance.Lead and manage a high-performing team to achieve outstanding results in pharmacovigilanceDevelop and implement effective strategies for PV planning,...

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...

OVERVIEW:The Junior Pharmacovigilance Specialist collaborates with the PV Solutions production team to analyze and report on safety parameters, within the context of patient safety against our clients' products, and in line with client requirements for case review.DESCRIPTION:Perform various tasks in support of our clients' clinical research including...

Excent Research is currently seeking to expand its Research and Development team for its Pharma Division. As part of this effort, we are actively recruiting for the positions of Pharmacovigilance Associates and Clinical Researchers. Eligibility: BSc, MSc, B Pharmacy, M Pharmacy, PharmD, Any UG / PG in Life Sciences **Job Types**: Full-time,...

**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...

Collect, review, and process adverse event reports from clinical trials, post-marketing sources, and literature. Ensure timely and accurate entry of safety data into safety databases (e.g., Argus, ARISg). Prepare and submit Individual Case Safety Reports (ICSRs) to regulatory authorities within stipulated timelines. Conduct follow-ups with healthcare...

**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...

We're Hiring:Salesforce Developer– Pune (Immediate Joiners Only)Are you a passionateSalesforce Developerwith 3–5 years of hands-on experience in building scalable Salesforce solutions?We're looking for talented professionals who canjoin immediatelyand contribute to our growing Salesforce practice.Location:Pune, IndiaExperience:3–5...