Safety Reporting

**Job Overview** - As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities._ Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs),...

**_IQVIA Biotech is seeking a Safety Specialist located in Mexico (Home Based) with prior CRO experience and a minimum of two years in clinical trial safety processing in Argus:_** **BASIC FUNCTION**: - Delivers Safety Management Department services according to ICH-GCP guidelines, regulatory requirements and IQVIA Biotech SOPs and/or project specific...

**Job Overview** **Essential Functions** - Assess Lifecycle Safety data for reportability to relevant authorities, including EudraVigilance, and track reportable cases. - Report to regulatory authorities, ethics committees, institutional review boards, investigators, and oversight groups per legislation, within timelines, and in a format compatible with...

**Job Overview**- As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities._Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and...

**Company Description**Etsy is the global marketplace for unique and creative goods. We build, power, and evolve the tools and technologies that connect millions of entrepreneurs with millions of buyers around the world. As an Etsy Inc. employee, whether a team member of Etsy, Reverb, or Depop, you will tackle unique, meaningful, and large-scale problems...

Job Overview Serve as principal owner of the SARA deliverable and have responsiblility for completion of the deliverable in compliance with all applicable service level agreements. Essential Functions - Act as primary author & or reviewer/QCer of SARA deliverables involving aggregate reports, signal management or literature review projects. - Lead, author...

The Scheduler plays a vital role in organizing and managing the schedules of motorcycle training sessions, instructors, participants, and resources to ensure that the training programs run smoothly and efficiently.**KEY RESPONSIBILITIES**:**Training Session Scheduling**:- Coordinate and schedule motorcycle safety training sessions, ensuring that they meet...

**_IQVIA Biotech _**_is seeking a Clinical Safety Specialist with at least 2 years of clinical trial case processing experience working in Argus:_ **BASIC FUNCTION**: - Delivers Safety Management Department services according to ICH-GCP guidelines, regulatory requirements and IQVIA Biotech SOPs and/or project specific procedures. - Primary responsibilities...

**Job Overview** We are seeking a dedicated and detail-oriented professional to join our team as a Operations Specialist 1. In this role, you will provide critical phone support to healthcare professionals and patients, handling medical inquiries, adverse events, product quality complaints, and other relevant calls. This position does not involve commercial...

As a Graduate Pharmacovigilance you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Review and process safety events (pre-marketing, post-marketing, medical device and drug) and/or other medically related information per assigned tasks and project...