Pharmacovigilance Associate

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health.Qualification & Specifications :MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T,...

About the Company Qinecsa is a trusted, global partners bringing together best-in-class technology and scientific expertise to connect life science companies, public health, and regulatory sectors to the right safety solutions. we take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services,...

About the CompanyQinecsa is a trusted, global partners bringing together best-in-class technology and scientific expertise to connect life science companies, public health, and regulatory sectors to the right safety solutions. we take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology,...

About the CompanyQinecsa is a trusted, global partners bringing together best-in-class technology and scientific expertise to connect life science companies, public health, and regulatory sectors to the right safety solutions. we take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology,...

Job Description - To lead a team of Drug Safety Physicians working on ICSRs Projects. - Conduct initial assessment and Medical Review of ICSR s into the safety database. - Review and verify appropriate selection of adverse events from source documents, check the seriousness criteria, appropriate MedDRA code, suspect drug, concomitant medications, lab data,...

Company Description We are PrimeVigilance part of Ergomed Group a specialised mid-size pharmacovigilance service provider 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 Affairs and...

**Job Location**: New Delhi, India **Requirements**: - At least 2 years of experience in quality assurance in GCP, preferably pharmacovigilance, in the CRO or pharmaceutical industry - Awareness of global regulatory and pharmacovigilance environment - Strong written and verbal communication skills - Willingness to work from job...

At Turacoz, we are a leading global provider of innovative healthcare communication solutions. We work with pharmaceutical companies, medical device manufacturers, research institutes, and healthcare organizations to deliver high-quality scientific writing, medical communications, regulatory writing, and digital marketing services. Our goal is to connect...

Role & responsibilities• Provide timely support for medical assessment of initial case triage and also assist in reviewing medical information queries pertaining to ICSRs. • Able to properly rank event based on seriousness criteria, labeling and causality assessment • Causality assessment for all events based on WHO algorithm and ICH guidelines also...

I am sharing with you the details related to the profile and the company below and kindly acknowledge this email with your updated resume:Company website : Company LinkedIn Page : Job Description for Argus Config. :Should have good understanding of the Pharmacovigilance/ Health Care domain.Should have excellent knowledge of Oracle Argus Safety/LSMV or other...