Safety Specialist

**_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 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...

**_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** Serve as principal owner of the SARA deliverable and have responsibility 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,...

**Job Overview****Essential Functions**- Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.- Perform pharmacovigilance activities, including collecting and tracking incoming adverse events (AEs) and endpoint information.- Determine initial/update status of incoming events, database entry, coding AEs and...

Viatris Healthcare México S. de R.L. de C.VAt VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthier at every stage of life.We do so via:Access - Providing high quality trusted...

**Job Overview**The Pharmacovigilance and Case Intake Specialist/Operations Specialist 1 reviews, assesses, and processes safety data. This role involves distributing reports/data to internal and external parties, following regulations, SOPs, and guidelines with support from senior team members.**Essential Functions**- Complete assigned training on time.-...

**Job Overview** Manage Safety staff responsible for Safety Operations processing in alignment with departmental and corporate standards. Contribute to Global initiatives. Work in close collaboration with SM and other relevant stakeholders supporting the achievement of local and global deliverables and metrics. **Essential Functions** - Work closely with...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

External Job Description **Job Overview** **Key Responsibilities** - Process Safety data as per regulations, guidelines, SOPs, and project requirements. - Perform Pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AE)/endpoint information, database entry, coding AE and Products, writing narratives, and more. - Assess...