Pharmacovigilance

TCS is hiring for Pharmacovigilance.Role: Pharmacovigilance.Work location: MumbaiExperience: 2 - 7 years relevant experience in PharmacovigilanceQualification: Graduate or Post- Graduate in Life Science (B.sc/ M.sc/ B.Pharm/ M.Pharm)Job Description:Ability to understand and analyses the complex data and performs the activities including accessing the...

TCS is hiring for Pharmacovigilance.Role: Pharmacovigilance.Work location: MumbaiExperience: 2 - 7 years relevant experience in PharmacovigilanceQualification: Graduate or Post- Graduate in Life Science (B.sc/ M.sc/ B.Pharm/ M.Pharm)Job Description:Ability to understand and analyses the complex data and performs the activities including accessing the case in...

TCS is hiring for Pharmacovigilance. Role: Pharmacovigilance. Work location: Mumbai Experience: 2 - 7 years relevant experience in Pharmacovigilance Qualification: Graduate or Post- Graduate in Life Science (B.sc/ M.sc/ B.Pharm/ M.Pharm) Job Description: Ability to understand and analyses the complex data and performs the activities including accessing...

A Pharmacovigilance Specialist will manage the Pharmacovigilance activities through follow-up call intake, documentation, and urgent responses to all PV correspondences from national authorities and business partners. He will be able to prepare all needed SOPs and policies related to PV activities and complete the PV audit. He will perform processing of...

Business: Piramal Critical Care  Department: Pharmacovigilance Location: Kurla, Mumbai Travel: Low   Job Overview: The Executive Pharmacovigilance will be responsible end-to-end case management, including case receipt, facilitation of case follow-up, case download from regulatory authority websites, database entry, peer review and submission to...

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...

Experience -10 - 12 yearsQualification Requirement -B.Pharm / M. PharmResponsibilitiesSupport and execute Pharmacovigilance related activities in UNICHEM Laboratories Limited.Prepare and maintain Pharmacovigilance documentation and SOPs and training to the relevant stake holdersTrain Pharmacovigilance team on standard operating procedure (SOP) and Work...

Experience - 10 - 12 years Qualification Requirement - B.Pharm / M. Pharm Responsibilities Support and execute Pharmacovigilance related activities in UNICHEM Laboratories Limited. Prepare and maintain Pharmacovigilance documentation and SOPs and training to the relevant stake holders Train Pharmacovigilance team on standard operating procedure (SOP)...

Experience - 10 - 12 yearsQualification Requirement - B.Pharm / M. PharmResponsibilitiesSupport and execute Pharmacovigilance related activities in UNICHEM Laboratories Limited.Prepare and maintain Pharmacovigilance documentation and SOPs and training to the relevant stake holdersTrain Pharmacovigilance team on standard operating procedure (SOP) and Work...

Experience - 10 - 12 yearsQualification Requirement - B.Pharm / M. PharmResponsibilitiesSupport and execute Pharmacovigilance related activities in UNICHEM Laboratories Limited.Prepare and maintain Pharmacovigilance documentation and SOPs and training to the relevant stake holdersTrain Pharmacovigilance team on standard operating procedure (SOP) and Work...

> A Pharmacovigilance Associate plays a crucial role in ensuring adherence to relevant regulations and standard operating procedures. Specializing in drug safety management, clinical trials, and medical supervision, their primary responsibilities include monitoring and reporting pharmacovigilance developments. They oversee processes to ensure the...

**Job description** **Responsibilities**: - Receive, review, and process adverse event reports and other safety information in accordance with established procedures and timelines. - Perform case assessment and documentation, including the identification of potential safety concerns and relevant medical information. - Ensure the quality and integrity of...

Business: Piramal Critical Care Department: Pharmacovigilance Location: Kurla, Mumbai Travel: Low **Job Overview**: The Executive Pharmacovigilance will be responsible end-to-end case management, including case receipt, facilitation of case follow-up, case download from regulatory authority websites, database entry, peer review and submission to applicable...

**Designation**: Pharmacovigilance Administrative Support **Education**: B pharm/Science Graduate. **Experience**: Fresher or experience as a trainer with Pharma Industry. **Salary**: Best in industry **Job Location**:BKC Mumbai - Coordinating for Pharmacovigilance Trainings for various Abbott affiliates across the globe. - Maintenance of Training...

)Review and conduct medical assessment of Human and Veterinary Pharmacovigilance/ safety documents (including ICSRs and aggregate safety reports such as PADER/PSUR). )Perform medical review of serious and non-serious ICSRs with importance on the causality, seriousness, expectedness, MedDRA coding etc. )Review of literature articles for identification of...

)Review and conduct medical assessment of Human and Veterinary Pharmacovigilance/ safety documents (including ICSRs and aggregate safety reports such as PADER/PSUR). )Perform medical review of serious and non-serious ICSRs with importance on the causality, seriousness, expectedness, MedDRA coding etc. )Review of literature articles for identification of...

**Pharmacovigilance** jobs involve monitoring, and assessing the risks and benefits of medicines to patients, so it's vital for anyone working in this profession that the information they work on is accurate. **A Medical Coder **transcribes patients records into an insurance-accepted coding system. With this information, they are able to process claims for...

**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...

**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...

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 training documents (i.e.,...