Drug Safety Reporting Specialist

Summarized Purpose: Provides administrative safety support to the safety reporting team and Pharmacovigilance department. Responsible for tasks related to receipt and submission of expedited and periodic safety reports, including quality check tasks, pertaining to the department’s projects. Assists with allocation of work tasks to safety reporting team...

Receives, prepares, and submits safety reports to applicable parties. Escalates to lead and line manager if any issues are encountered. Ensures reports are submitted in compliance with regulatory timelines and country legislation. Assists in producing metrics and alerts the manager to quality or timeline issues. Participates in project teams and may lead...

Job Description **Summarized Purpose**: Provides administrative safety support to the Pharmacovigilance department. Specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. This includes other general administration tasks such as filing, photocopying, typing and performing reconciliation...

**_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...

**_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...

**Be part of our dynamic community and make a real impact on our clients' success. Assistantly offers some of the best benefits and perks in the industry.** **Unicorn Role Overview**:Do you have a talent for promoting safety and ensuring smooth operations? As a Safety Administrator, you'll be the driving force behind our client's safety programs, ensuring...

Performs day-to-day Pharmacovigilance (PV) activities within a highly regulated environment and driven by strict timelines. PV activities include but are not limited to collection, monitoring, assessment, evaluation, research and tracking of safety information. - Coordinates and performs PV activities such as data entry, coding and assessment of adverse...

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IQVIA Biotech, a global full service CRO providing flexible and tailored clinical solutions to smaller biotech companies, is seeking additional talent within our **Site File Operations team**. Our **Site File Specialist II **opportunity requires: BS/BA/BSc, or equivalent, plus 2 years of related experience; regulatory document review experience preferred....

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The person we are looking for must have excellent ENGLISH written and oral skills, as there will be a good amount of communication with our internal teams and clients. You will be responsible for campaign implementation, performance reporting, and ensuring this arm of lead generation is running cohesively with our clients' other marketing...