Pharmacovigilance(Pv) Associate Fresher

Pharmacovigilance is science and practises involved in the identification, evaluation, comprehension, and mitigation of side effects and other medical/vaccination-related issues are referred to as harmacovigilance. Before being approved for use, all medications and vaccines go through extensive clinical trials to test their safety and...

Excent Research is currently seeking to expand its Research and Development team for its Pharma Division. As part of this effort, we are actively recruiting for the positions of Pharmacovigilance Associates and Clinical Researchers. Eligibility: BSc, MSc, B Pharmacy, M Pharmacy, PharmD, Any UG / PG in Life Sciences **Job Types**: Full-time,...

> 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** - 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...

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...

**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...

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...

**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...

**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...

**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...

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...

Processing adverse events reports from post marketing sources into Teva's global safety database: - The different sources / types of reports includes: Reports from the scientific literature, Teva partners (other pharmaceutical companies), Health Authorities, Non-interventional studies and other programs - The processing includes Adverse Events coding (in...

Provide medical and clinical guidance to managers before, throughout, and following clinical trials. - Maintain consistency of safety assessments. - Perform a variety of safety assessments. - Serve in cross-functional teams as a medical and scientific representative. - Ensure regulatory compliance and safety throughout trial. - Submit periodic reports to the...

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...

**Team Lead - CDM/PV** **Qualification**: Graduate/Post Graduate/ Doctorate degree in life sciences/Pharmacy/Medical sciences/Registered Nurse ** Responsibility**: **Business/ Customer**: - Minimal Customer interaction under guidance. - Understands Domain Process/sub process, functions, terminologies (such as SOP, QC checklists). - For PV/Complaints...

Sample responsibilities for this position include: Daily activities involve Have in-depth product knowledge, serve as product point of contact, and support Safety Management Team deliverables Partner with team members, stakeholders including Medical Safety Officer (MSOs), and a vendor Strategically plan and ensure timely, quality reports/safety analyses...

Name of post: International inbond voice process associate Fresher No of Post:3 Experience : 0-1 year. Location : Hinjewadi Education: Any Graduate Skill Required : Excellent communication and interpersonal skills call us / whats aap us 8208632580 /7517948509 **Job Types**: Full-time, Fresher **Salary**: ₹200,000.00 - ₹400,000.00 per...

Associate KPO **Location: - Magarpatta, Shirwal Satara Road** Experience: - Fresher or 1 Year Experience Qualification: - B.Com Graduate Skills: - Basic Knowledge of Computer like Excel, Documentation work fast in Excel. **Job Types**: Full-time, Fresher **Salary**: ₹214,110.00 - ₹300,000.00 per year Schedule: - Day shift - Monday to Friday -...

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