Deloitte Life Sciences Veeva R&D Consultant in Jersey City, New Jersey
Life Sciences Veeva R&D Consultant
The ConvergeHEALTH consulting team offers a startup feel within a larger firm. As part of the team, you will work with clients, the product teams, and the ConvergeHEALTH internal team. Through your client-facing efforts, you will have the opportunity to work directly with client and implementation team leadership to identify opportunities for digital health solutions, define project roadmaps, and implement innovative solutions developed by our ConvergeHEALTH product teams as well as leading industry solution providers.
Work you'll do
The professionals in ConvergeHEALTH understand the unique challenges confronting today's Life Sciences organizations. Our approaches are pragmatic and realistic, and span the continuum from new R&D operating models through portfolio management, clinical transformation, data analytics, IT transformation, and regulatory and safety considerations.
We help clients unlock business agility and sustainable value through technology. We reimagine the technology + business relationship by architecting future business and technology strategies, operating models, platforms, ecosystems, and capabilities into integrated business solutions. We orchestrate the breadth of Deloitte to co-create business value across the C-suite and to the board.
Deloitte has established a leadership position in the area of R&D Consulting. We have built outstanding insights to the challenges and opportunities in this space and have strong industry relationships and experiences in delivering business results. As we grow our alliance with Veeva, one of the leading software solution providers in the Life Sciences industry, we are looking for Consultants to help us shape the direction of our Veeva practice capabilities and delivery of project results. The ideal candidate should have deep functional and/or technical expertise of one of the Veeva suite of products (CTMS, eTMF, EDC, RIM, MedComms) and understands the needs of industry and regulators.
Bachelor's Degree or equivalent experience
Demonstrated understanding of Life Sciences R&D organizations and the drug development process, specifically as it relates to clinical development
Demonstrated aptitude in technology and an understanding of how to apply existing or new innovative technology solutions to core Life Sciences R&D processes.
Experience with any or all of the following Veeva products: CTMS, eTMF, EDC, RIM, Vault MedComms
Experience with all phases of Agile technology implementation projects
Experience working on distributed teams in an onshore/offshore delivery capacity.
Experience working on teams to develop business requirements, user stories, functional designs, process designs (including scenario design, flow mapping), prototyping, testing, and training.
Functional knowledge and experience of Clinical operations, clinical data management and/or regulatory domain.
Previous experience working on a Veeva Vault platform implementation project or certification in Veeva Vault is desirable but not required
Limited Sponsorship may be available
Ability to travel 20%, on average, based on the work you do and the clients and industries/sectors you serve
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.