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...

The primary duty of a Drug Safety Associate involves the ongoing monitoring and evaluation of adverse effects and safety concerns associated with drugs and medical products following market approval. As a Drug Safety Associate, your responsibilities will include monitoring, assessing, and reporting adverse events related to pharmaceutical products. You will...

Drug safety experts have numerous responsibilities and this can vary from one company to another. The roles include activities like. - Processing and writing of adverse event program - Follow up on important case reports - Serving as a link between company and the patients or healthcare experts to provide valid information on product safety. - Conducting...

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...

Role – Drug Safety Physician.Designation – Sr. Executive.Location – Pune.Qualification – MBBS/MD (Pharmacology).Experience – 2 to 7 Years (ICSR)Mode - Work from Office. (Kolkata)Notice Period – Immediate joiners preferred.CTC- Upto 25 LPAPosition Purpose:To Analyze, Review and Interpret Safety data.Primary Responsibilities:To Perform medical...

Job Description `Overview of the Organization Oracle 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...

Role – Drug Safety Physician.Designation – Sr. Executive.Location – Pune.Qualification – MBBS/MD (Pharmacology).Experience – 2 to 7 Years (ICSR)Mode - Work from Office. (Kolkata)Notice Period – Immediate joiners preferred.CTC- Upto 25 LPAPosition Purpose: To Analyze, Review and Interpret Safety data. Primary Responsibilities:To Perform medical...

Role – Drug Safety Physician.Designation – Sr. Executive.Location – Pune.Qualification – MBBS/MD (Pharmacology).Experience – 2 to 7 Years (ICSR)Mode - Work from Office. (Kolkata)Notice Period – Immediate joiners preferred.CTC- Upto 25 LPAPosition Purpose: To Analyze, Review and Interpret Safety data. Primary Responsibilities:To Perform medical...

Role – Drug Safety Physician. Designation – Sr. Executive. Location – Pune. Qualification – MBBS/MD (Pharmacology). Experience – 2 to 7 Years (ICSR) Mode - Work from Office. (Kolkata) Notice Period – Immediate joiners preferred. CTC- Upto 25 LPA Position Purpose: To Analyze, Review and Interpret Safety data. Primary...

Pharmacovigilance associates have a wide range of responsibilities, which can include: - 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...

**Typical Responsibilities Include** - 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...

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...

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...

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...

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...

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...