Drug Safety Associate

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,...

We're seeking dedicated individuals to join our Drug Safety team as Entry-Level Drug Safety Associates. This role offers an exciting opportunity for recent graduates to kickstart their careers in pharmacovigilance and drug safety. **Responsibilities**: - Assist in collecting, processing, and evaluating adverse event reports and safety data. - Ensure...

TCS is hiring for PV Drug Safety! Role: Pharmacovigilance Work location: Mumbai Experience: 1 - 7 years’ relevant experience in Pharmacovigilance Qualification: 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...

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...

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...

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 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...

Pune, India - DOP - 3054661 **Job Description**: **Technical/Functional Competency** 1) Sound Knowledge of Human Anatomy & Physiology - 2) MedDRA Coding & subsuming of adverse drug reaction/AE terms - 3) Seriousness determination - 4) Familiarity with pharmacological concepts - 5) Command on verbal and written communication skills - 6)Team Player Roles &...

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...

A pharmacovigilance associate **monitors all products and conducts post-market evaluations to ensure drug safety**. These experts are actively involved in assessing adverse event writings, updating reports on safety, conducting quality and conveying drug related case reports to appropriate authorities In summary, typical roles and responsibilities include...

A Pharmacovigilance Associate plays a crucial role in ensuring adherence to relevant regulations and standard operating procedures. They oversee processes to ensure the effectiveness of drugs while minimizing adverse effects in both research trials and hospital settings. **Responsibilities**: - recording and reporting adverse reactions received from...

Labcorp Drug Development As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired...

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...

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...