Drug Safety Specialist

TCS is hiring for PV Drug Safety!Role: PharmacovigilanceWork location: MumbaiExperience: 1 - 7 years’ relevant experience in PharmacovigilanceQualification: Bpharm/ Mpharm/ BHMS/ BAMS/ BDS/ Msc (Biotechnology, Zoology)Job Description:*Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code...

TCS is hiring for PV Drug Safety!Role: PharmacovigilanceWork location: MumbaiExperience: 1 - 7 years’ relevant experience in PharmacovigilanceQualification: Bpharm/ Mpharm/ BHMS/ BAMS/ BDS/ Msc (Biotechnology, Zoology)Job Description:*Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code...

Drug safety associates have a wide range of responsibilities, which can include: - Reviewing adverse event reports, safety data sheets, and physician advisories to identify potential risks associated with a particular drug - Conducting site visits to observe the distribution process to ensure compliance with federal regulations - Monitoring compliance with...

Drug safety associates have a wide range of responsibilities, which can include: - Reviewing adverse event reports, safety data sheets, and physician advisories to identify potential risks associated with a particular drug - Conducting site visits to observe the distribution process to ensure compliance with federal regulations - Monitoring compliance with...

A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they're on the market. Using standardised guidelines, they determine whether the medication causes any adverse reactions in patients and report their findings back to the pharmacovigilance department. **Job Types**: Full-time, Regular / Permanent,...

Job Description`Overview of the OrganizationOracle Life Sciences GIU (LSGIU) provides industry leading solution to Life Sciences organizations including pharmaceutical companies, CROs (Contract research Organizations), Academic research and Healthcare providers that include care providers, IDN (integrated delivery networks), public regional/national...

A career in pharmacovigilance provides good prospects with generation of new drugs every day. Pharmacovigilance is the process of collecting, researching, monitoring, evaluating and assessing information derived directly or indirectly from patients. **Job Types**: Full-time, Regular / Permanent, Fresher **Salary**: ₹15,000.00 - ₹25,000.00 per...

The Pharmacovigilance Specialist collaborates with the Lit Search/Medical Writing team and clients to analyze and report on safety findings, within the context of patient safety and efficacy against our clients’ drugs and products. The Pharmacovigilance Specialist ensures effective and clear documentation and communication of safety information, to share...

The Pharmacovigilance Specialist collaborates with the Lit Search/Medical Writing team and clients to analyze and report on safety findings, within the context of patient safety and efficacy against our clients’ drugs and products. The Pharmacovigilance Specialist ensures effective and clear documentation and communication of safety information, to share...

The Pharmacovigilance Specialist collaborates with the Lit Search/Medical Writing team and clients to analyze and report on safety findings, within the context of patient safety and efficacy against our clients’ drugs and products. The Pharmacovigilance Specialist ensures effective and clear documentation and communication of safety information, to share...

The Pharmacovigilance Specialist collaborates with the Lit Search/Medical Writing team and clients to analyze and report on safety findings, within the context of patient safety and efficacy against our clients’ drugs and products. The Pharmacovigilance Specialist ensures effective and clear documentation and communication of safety information, to share...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

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...

Preparing reports of adverse drug reactions that may involve complex medical terminology, medical chart reviews, and statistical analyses - Responsible for monitoring potential side effects of drugs being marketed in the United States by reviewing case studies and medical literature - Assisting in processing insurance claims for drug products dispensed by...

recording and reporting adverse reactions received from healthcare professionals and consumers - conducting in-depth interviews with patients and healthcare professionals - developing a thorough knowledge of products - completing periodic safety update reports on drugs and other treatments - writing and reviewing serious adverse effects reports and forms -...

recording and reporting adverse reactions received from healthcare professionals and consumers - conducting in-depth interviews with patients and healthcare professionals - developing a thorough knowledge of products - completing periodic safety update reports on drugs and other treatments - writing and reviewing serious adverse effects reports and forms -...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...