Pharmacovigilance Associate

Job OverviewThe Pharmacovigilance Services Associate position at Lifelancer is an exciting opportunity to work with a global professional services company that offers Strategy and Consulting, Technology and Operations services.In this role, you will be aligned with our Life Sciences R&D vertical and be part of one of the sub-offerings - Clinical,...

Job description WHO defines Pharmacovigilance (PV) as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. Pharmacovigilance is also known as drug safety and it focuses on ADR (Adverse drug reaction).The main aim of Pharmacovigilance is to monitor approved drugs...

About LifelancerLifelancer is a talent-hiring platform in Life Sciences, Pharma and IT that connects talent with opportunities.Job Description:We are seeking a Pharmacovigilance Associate Specialist to join our team. As a key member of our team, you will be responsible for creating and managing case identification, data entry, MedDRA coding, case processing,...

About the RoleThis is an exciting opportunity to join our team as a Pharmacovigilance Services Associate in Bengaluru, Karnataka, India. As a key member of our Life Sciences RD vertical, you will be responsible for managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database.Key...

Job Overview:We are seeking a skilled Clinical Trials Operations Manager to lead our pharmacovigilance team in Bangalore. The successful candidate will be responsible for managing the day-to-day operations of the team, ensuring compliance with regulatory requirements and providing high-quality service to clients.The ideal candidate will have experience in...

About the RoleThis is a dynamic opportunity to join our team as a Pharmacovigilance Services New Associate. You will be aligned with our Life Sciences RD vertical, where you will contribute to pharmacovigilance and patient services solutions.As a key member of our team, you will be responsible for managing case identification, data entry, MedDRA coding, case...

About the JobWe are seeking a skilled Pharmacovigilance Services New Associate to join our team at Lifelancer. The successful candidate will be responsible for creating and managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global...

Job DescriptionWe are seeking a highly skilled Pharmacovigilance Specialist to join our team as a Literature Searching Expert. In this role, you will be responsible for conducting complex research and analysis to produce high-quality search results for clients.Key Responsibilities:Develop and refine literature search strategies and methodologies to ensure...

About the Role:As a Life Sciences Regulatory Associate at Lifelancer, you will play a critical role in ensuring the compliance and regulatory requirements of our clients in the pharmaceutical and biotechnology industries.The ideal candidate will have a strong understanding of pharmacovigilance principles and practices, with experience in case management,...

We are currently seeking a Junior MICC Associate to join our growing team. Working within the Medical Information Contact Centre (MICC) for the Pharmacovigilance function you will: - Follow both global and local regulations to protect personal and client related data as per company policy. - Be required to always exhibit a detail-oriented etiquette and...

Advarra is a leader in the clinical research industry, providing innovative solutions to accelerate trials and advance human health.We are seeking a Senior Clinical Research Associate to join our team. This role will be based in Bengaluru, India and can be performed remotely or in-office.The successful candidate will have 6+ years of experience in clinical...

About the RoleWe are seeking a highly skilled Research Associate II to join our team. This role is ideal for someone with experience in clinical research and a strong understanding of industry regulations.Job DescriptionThe Research Associate II will be responsible for designing and developing calendars, budgets, and case report forms for clinical trial...

Job SummaryWe are seeking a Clinical Safety Associate to join our team as a Narrative Writer. This role involves managing and developing individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports.About the RoleIn this position, you will be responsible for supporting clinical submission narrative writing...

We are seeking a drug physician in Biocon Biologics Pharmacovigilance who independently or in association with senior physicians will be responsible for continuous evaluation of the safety profile of company products through adverse event monitoring, supporting clinical trial PV safety activities, overseeing aggregate report reviews, safety signal and risk...

We are seeking a drug physician in Biocon Biologics Pharmacovigilance who independently or in association with senior physicians will be responsible for continuous evaluation of the safety profile of company products through adverse event monitoring, supporting clinical trial PV safety activities, overseeing aggregate report reviews, safety signal and risk...

We are seeking a drug physician in Biocon Biologics Pharmacovigilance who independently or in association with senior physicians will be responsible for continuous evaluation of the safety profile of company products through adverse event monitoring, supporting clinical trial PV safety activities, overseeing aggregate report reviews, safety signal and risk...

Responsibilities: - Develop and deliver training on Clinical Research, Clinical Data Management (CDM), Pharmacovigilance (PV), and Good Clinical Practice (GCP), with additional knowledge of Medical Writing (MW) and Regulatory Affairs (RA) as a plus. - Conduct assessments and provide feedback to improve trainees’ clinical research skills. - Stay updated on...

About LifelancerLifelancer is a talent-hiring platform connecting professionals with opportunities in life sciences, pharma, and IT. We bridge the gap between talented individuals and exciting job openings.Job OverviewWe are currently seeking a skilled Pharmacovigilance Services Associate to join our team. This role involves managing clinical submissions,...

Associate Safety Operations Adviser **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department**: Global Safety.- **About the Department** - Global Safety, Bangalore has global responsibility for surveillance of Safety and Quality of Novo Nordisk clinical development and marketed Products and is responsible for...

Associate Safety Operations Advisor **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department**: Global Safety.- **About the Department** - Global Safety, Bangalore has global responsibility for surveillance of Safety and Quality of Novo Nordisk clinical development and marketed Products and is responsible for...