Location: Basking Ridge,NJ, USA
Job Title: Veeva Solutions Architect Job Function: Solutions Architecture Job Type: W2 to G3 Tech Consultants (No other benefit than hourly rate) Only GC or Citizen Location: Basking Ridge, NJ 07920 (Hybrid- on site as required) Contract: 12 months Note: Candidate needs to Sign Non-Compete and agree to work with the contract duration. Scope of Job •The Veeva Solutions Architect is a senior client facing role. The Veeva Solutions Architect will be responsible for leading the design and functional workstreams on implantation and enhancement projects on medium to large scale engagements Primary Responsibilities •Collaborate with project team members to architect solutions per Business Requirements. •Perform analysis and design (functional/non-functional) activities to create clinical/Regulatory solution landscapes for our Life Sciences Clients. •Take complex concepts and articulate them to an audience of varying levels of expertise and subject matter expertise. •Provide direction to junior team members and support recruitment efforts. •Grow the capabilities of the team, develop best practices and accelerators. •Create high-quality assessments, health checks and clinical architecture, in support of solution design. •Recommend risk-based solutions to solve business needs. •Lead Solution review sessions and provide input to change control review and approval processes. Qualifications •Have a proven track record leading discussions with senior management and executives as the subject matter expert. •10+ years of experience designing and delivering Clinical and Regulatory GxP and non-GxP IT solutions. •Extensive Veeva Development Cloud background and demonstrated understanding of the key processes and sub-processes specific to Life Sciences. •Strong understanding of system and data security principles and best practices. •Willingness to wear any hat that is necessary to drive customer success. •Continue to extend subject matter expertise in the life sciences industry and learn Veeva Solutions. •Strong understanding of system and data security principles and best practices. •Good functional knowledge of Life Sciences Market Authorization processes. •Ability to communicate efficiently with technical and non-technical staff and members of interdisciplinary teams both verbally and in writing. •Keen attention to detail and proven analytical and problem-solving abilities. •Ability to handle multiple priorities and work under pressure. •Excellent problem-solving skills. •The following Qualifications are Required: o Expertise in Veeva RIM, Veeva Submissions, Archive, Veeva QMS, Veeva Quality Docs ••The following Qualifications are preferred: o Experience with Regulatory Affairs Strategy, Intelligence, Regulatory Information Mgt & Operations, and/or Submission Publishing domains in support of market authorization. o Experience with Audits, Inspections, Vendor Oversight, and issues management such as SSNs. CAPA, and risk management. o Experience with Architecture Frameworks/Processes (e.g. TOGAF) and help define patterns and other architectural accelerators. Education & Certifications •Bachelor's Degree