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Expired
  • Location: Boston
  • Salary: $To be Discussed. Benefits include bonus, 401K, PTO, heath insurances and more
  • Job Type:Permanent

Posted over 1 year ago

Our client is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Their team’s knowledge of science and expertise in technology help them better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.

They operate a people first culture, where there is strong collaboration, employee growth and retention. They anticipate the US operation will double in size in the next year or so. This offers a great time to join to make an impact on your career.

Overview:
The individual will be responsible to support strategic projects for R&D division at Pharmaceutical and Biotech customers and mainly on Veeva Vault platform. The individual will provide the technical and delivery management skills required to analyze customer needs and gaps to propose and implement solutions for the desired state. You will have to work with Business Users and Managers of Customers in conjunction with the internal team.

Responsibilities:
• Review Business processes and systems
• Implement configurations within Veeva Vault
• Develop recommendations and future state strategy
• Perform Gap Analysis, Define Future state process workflow, Resolve user issues.
• Produce and deliver required technical documents and reports to customers

Qualifications/Experience required:
• Strong Experience with Veeva Vault Platform including QMS, eTMF, etc.
• Experience with content creation, content management and deployment
• Certification on Veeva (preferred)
• Project Management skills including Resource & Effort Planning, Task Planning & Scheduling, Scope & Time Management, and Vendor Management and Risk Assessment.
• Strong understanding of R&D process and experience handling scientific / clinical informatics projects.
• Ability to prioritize requirements, handle escalations, guide the team and remove blockers
• Knowledgeable about the Pharmaceutical Research and Drug Discovery & Development processes and Biologics workflows.
• Knowledge on standard and policies including 21CFR part 11, GLP, GCP etc.

Location:
The primary office location will be from remote.
Multiple Locations - Boston, Raleigh, or Toronto