Play a vital role in safeguarding patient safety by driving excellence in pharmacovigilance documentation.
Proclinical is seeking a Sr. PV Scientist, Quality Document Associate to support quality assurance activities within the cardiovascular and pharmaceutical sectors. This role focuses on ensuring high-quality documentation and supporting process improvements in pharmacovigilance operations.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
Conduct quality control (QC) reviews of documents to ensure accuracy and compliance with established standards.
Collaborate with internal teams and external vendors to maintain high-quality deliverables.
Support process improvement initiatives to enhance operational efficiency.
Assist with vendor management activities to ensure alignment with organizational goals.
Manage and maintain SharePoint or other document management systems as required.
Key Skills and Requirements:
Strong attention to detail and ability to perform thorough quality reviews.
Familiarity with pharmacovigilance processes and regulatory requirements.
Proficiency in managing documentation systems such as SharePoint.
Excellent communication and collaboration skills to work effectively with cross‑functional teams.
Ability to support process improvement and vendor management activities.
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Proclinical is seeking a Sr. PV Scientist, Quality Document Associate to support quality assurance activities within the cardiovascular and pharmaceutical sectors. This role focuses on ensuring high-quality documentation and supporting process improvements in pharmacovigilance operations.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
Conduct quality control (QC) reviews of documents to ensure accuracy and compliance with established standards.
Collaborate with internal teams and external vendors to maintain high-quality deliverables.
Support process improvement initiatives to enhance operational efficiency.
Assist with vendor management activities to ensure alignment with organizational goals.
Manage and maintain SharePoint or other document management systems as required.
Key Skills and Requirements:
Strong attention to detail and ability to perform thorough quality reviews.
Familiarity with pharmacovigilance processes and regulatory requirements.
Proficiency in managing documentation systems such as SharePoint.
Excellent communication and collaboration skills to work effectively with cross‑functional teams.
Ability to support process improvement and vendor management activities.
#J-18808-Ljbffr
Sr. PV Scientist, Quality Document Associate Arbeitgeber: Proclinical Staffing
Proclinical ist ein hervorragender Arbeitgeber, der Ihnen die Möglichkeit bietet, einen echten klinischen Einfluss zu nehmen und gleichzeitig das Wachstum im Bereich fortschrittlicher kardiologischer Lösungen in Österreich zu leiten. Mit einem wettbewerbsfähigen Gehalt, strukturierten Schulungs- und Entwicklungsmöglichkeiten sowie einem unterstützenden Arbeitsumfeld fördert Proclinical eine engagierte Unternehmenskultur, die Teamarbeit und persönliche Weiterentwicklung schätzt. Darüber hinaus profitieren Sie von großzügigem Urlaub, zusätzlichen Wohlfühltagen und Initiativen zur psychischen Gesundheit, die das Wohlbefinden der Mitarbeiter in den Vordergrund stellen.
