Veeva Quality Assurance Specialist
4 weeks ago
Job Summary
The Perelman School of Medicine at the University of Pennsylvania seeks a highly skilled Regulatory Affairs Veeva Quality Assurance Specialist to join our team. As a key member of our Clinical Research Unit, you will be responsible for reviewing and migrating Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
Key Responsibilities
- Review and itemize regulatory documentation from the current document management system to ensure accuracy and completeness.
- Migrate the created document inventory to the SiteVault platform, including person, organization, product, and study profiles, via bulk document transfer.
- Map existing data to unique Veeva data fields and assign metadata for new data fields.
- Collaborate with the Veeva Quality Assurance Lead to ensure seamless integration and quality assurance of the migrated data.
Qualifications
- Bachelor's degree in a life science or human subject protection field, with 3-5 years of research experience and at least 2 years of regulatory experience.
- Strong problem-solving and critical thinking skills, with effective communication and writing skills.
- Ability to work independently and as part of a team, with a high level of general computing ability and intermediate/expert level of function in Microsoft Office applications.
What We Offer
- A competitive salary range of $51,824.00 - $63,600.00 Annual Rate.
- A comprehensive benefits package, including health, life, and flexible spending accounts, tuition assistance, retirement plans, and time away from work.
- A fast-paced and dynamic work environment with opportunities for professional growth and development.
How to Apply
Please submit your application, including your resume and cover letter, to [insert contact information]. We look forward to hearing from you
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