Drug Safety Associate Professional

Job Summary:Parexel is seeking a highly skilled Senior Drug Safety Physician to join our team. As a key member of our Pharmacovigilance department, you will be responsible for providing medical review, analysis, and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational and marketed...

About the RoleTransform Drug Safety and Pharmacovigilance at Veeva Systems! We seek Drug Safety and Pharmacovigilance professionals to join our Professional Services team, supporting Vault Safety implementations for life sciences customers. Collaborate with innovative thinkers and challenge the status quo with new technology!What You'll DoSupport customers...

The RoleTransform and innovate with Veeva Systems as we seek Drug Safety and Pharmacovigilance experts to join our Professional Services team. We want innovative thinkers with deep domain expertise who are ready to challenge the status quo with new technology.As a key member of our Professional Services team, the Consultant – Safety will work side-by-side...

Job Purpose:Provide medical review, analysis, and guidance during the drug safety reporting cycle.Assess the clinical relevance of medical data and provide medical advice to team members.Maintain a good working knowledge of drug safety regulations and guidelines.Responsibilities:Perform medical review of cases according to SOPs and liaise with clients.Assess...

About the Role:We are seeking a skilled Medical Review Specialist - Pharmacovigilance to join our team at Parexel.Responsibilities:Perform medical review of cases according to client Standard Operating Procedures (SOPs) and liaise with the client, as required.Write Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assess company...

Job SummaryOracle Life Sciences is seeking a highly skilled Principal Consultant with expertise in Argus Drug Safety Data Migration to join our team. As a key member of our Life Sciences Technical Consulting (LSTC) group, you will be responsible for delivering high-quality services to our customers worldwide.The ideal candidate will have a strong background...

Transform Drug Safety and Pharmacovigilance with VeevaHelp us revolutionize the industry by joining our Professional Services team as a key member. As a Drug Safety and Pharmacovigilance expert, you will support the implementation of our Vault Safety solution, working closely with customers and senior consultants to deliver innovative...

Company OverviewPharma Stuff, a leading pharmaceutical manufacturing company, is dedicated to innovation and quality in the production of life-saving drugs. With a strong presence in the Pharmaceutical Manufacturing industry, our firm employs over 1000 professionals focused on excellence. We promote growth by nurturing talented individuals from within our...

About the RoleVeeva is seeking a skilled Safety Consultant to support the implementation of our Vault Safety solution. As a key member of our Professional Services team, you will work closely with customers and senior consultants to deliver successful projects.ResponsibilitiesSupport life sciences customers in the rapid configuration and implementation of...

Company Overview: Veeva Systems is a leading provider of cloud-based software solutions for the life sciences industry. Our Professional Services team supports customers in implementing our Vault Safety solution, a cutting-edge platform for drug safety and pharmacovigilance.Job Description: We are seeking an experienced Senior Safety Systems Implementation...

The RoleTransform and innovate with Veeva's Professional Services team to bring cutting-edge solutions to Drug Safety and Pharmacovigilance.We're seeking experts to join our team and support the implementation of our Vault Safety solution.As a Consultant – Safety, you'll work closely with customers and senior consultants to deliver exceptional results.Key...

Job SummaryWe are seeking an Associate Safety Scientist to support the Expedited Safety Reporting team at Bristol Myers Squibb. As an Associate Safety Scientist, you will play a key role in ensuring the quality and integrity of safety data, working closely with safety scientists and medical review safety physicians to expedite the processing of SUSAR...

Job SummaryThe Worldwide Patient Safety group at Bristol Myers Squibb is responsible for ensuring the safety of our medicines. This includes all pharmacovigilance and pharmaco-epidemiology deliverables, including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy, and...

Job SummaryThe Expedited Safety Reporting (ESR) Scientist is responsible for ensuring the timely and accurate reporting of safety information to regulatory agencies worldwide. This role requires strong analytical and communication skills, as well as the ability to work effectively in a team environment.Key ResponsibilitiesPrepare high-quality narrative...

Job SummaryThe Expedited Safety Reporting (ESR) Scientist is a key member of the Worldwide Patient Safety (WPS) team at Bristol Myers Squibb (BMS). This role is responsible for ensuring the accuracy and quality of safety information in ESRs submitted to regulatory agencies worldwide.Key ResponsibilitiesPrepares high-quality narrative summaries for expedited...

Job SummaryWe are seeking a highly skilled Safety Scientist to join our Expedited Safety Reporting team at Bristol Myers Squibb. As a key member of our team, you will play a critical role in ensuring the safety of our medicines and adhering to global regulatory requirements.Job ResponsibilitiesPerform high-quality data entry of Individual Case Safety...

Job DetailsThis is a Medical Data Safety Specialist role where you will be part of the Pharmacological Department. Your key responsibility will be to report adverse effects and side effects, in accordance with current Dutch and European legislation for pharmacology.You may also train colleagues in departments such as marketing and sales, medical and clinical...

Job DescriptionWe are seeking a skilled and detail-oriented professional to join our team as a Safety Data Reconciliation Lead. In this critical role, you will be responsible for ensuring the quality and accuracy of adverse event reports, as well as navigating the intricacies of our drug safety databases to process adverse event reports.Key...

About the RoleThe Worldwide Patient Safety group at Bristol Myers Squibb is responsible for ensuring the safety of our medicines. As a Safety Specialist, Regulatory Compliance, you will contribute to pharmacovigilance and pharmaco-epidemiology deliverables, including single case and aggregate safety monitoring, safety reporting, and risk management...

Job SummaryWe are seeking an experienced Associate Director, Medical Safety Review to join our team at Bristol Myers Squibb. This role will be responsible for providing high-quality medical review of Individual Case Safety Reports (ICSRs) and supporting signal detection and risk management activities.Key ResponsibilitiesProvide medical assessment of ICSRs...