Solution Consultant R&D LatAm

Há 1 mês

São Paulo, Brasil Veeva Systems Tempo inteiro

The Role


Do you want to help sales of leading cloud solutions in the Life Sciences space? Interested in developing sales and demo skills? As one of the members of our Veeva Solution Consulting team, you will be responsible for supporting the sales process by understanding our customer’s business needs and matching the Vault solution that best meets the customer’s vision. At Veeva, we offer excellent opportunities for our people to capitalize on their skills and grow in the dynamic, unique, and exceptional work environment. You will be demonstrating our R&D Suite for Clinical Operations, Regulatory or Quality areas. 
Opportunities are available within Mexico and Brazil for this role. This is a work-anywhere, full-time permanent position with Veeva. 

What You’ll Do

Analyzing and understanding customer requirements Configuring and delivering solution demonstrations Using experience to guide customers to a best-in-class solution Providing solution-oriented responses to Requests for Proposals/Information (RFPs/RFIs) Preparing and delivering presentations aligned to RFP/RFI responses Leading Workshops, Conference Room Pilots (sandbox exercises) and Proof of Concepts  Working with cross-functional team members to ensure customer success and deliver value Support marketing activities such as recording videos, presenting webinars, attending conferences

Requirements

College Degree (Life science, computer science, or related degree)  2+ years of experience working with or for life sciences companies; including, Pharmaceutical, Biotechnology, Healthcare, and Medical Device and Diagnostics organizations with knowledge of document and data control and storage. Experience in pre-sales or similar customer roles for a software company Experience in one of the following areas: Clinical (TMF, CTMS, CRA), Regulatory Affairs, Regulatory Operations or Pharmacovigilance, Quality: Understanding of quality requirements, compliance considerations and processes for Quality process and content management, life sciences compliance, and/or computer systems validation Excellent English communication skills – written, verbal, and formal presentation Ability to act with speed to understand requirements, and create corresponding demonstrations of R&D solutions that meet customer expectations Ability to travel Driven self-starter, able to work independently

Nice to Have

Life Science, computer science, or related degree Knowledge of drug development processes SaaS/Cloud solutions and software technology experience Experience in consulting or project implementation Master’s Degree Experience with software solutions for at least one of the following systems: Clinical trials systems: Direct experience with systems such as DataTrak, Oracle Siebel, goBalto, BioClinica CTMS, Medidata Rave CTMS/Strategic Monitoring, Parexel IMPACT, Bio-Optronics Clinical Conductor, PhlexEView, Trial Interactive, DrugDev Site Selection and Payments, WingSpan eTMF and SiteZONE, Complion, Florence eBinders, Forte Oncore and eReg, Veeva Vault, NextDocs, Documentum, other clinical technologies Regulatory systems: Direct experience with systems such as Veeva Vault, Organex, Ultreia, Lorenz, PAREXEL/LIQUE NT, Insight, CSC Regulatory Tracker, ArisGlobal Register, and other regulatory information management or submissions systems. Quality systems: Veeva Vault, SoftExpert, ETQ Reliance, TrackWise, OpenText, MasterControl, SharePoint, Documentum, FirstDoc FirstPoint, NextDocs, UL ComplianceWire, and other quality information management or content management systems

Perks & Benefits

Work Remotely Flexible PTO Allocations for continuous learning and development Health and wellness programs

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