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.
If you are having difficulty in applying or if you have any questions, please contact Joshua Bye at j.bye@proclinical.com.
Apply Now:
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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