Description
Reference #: 915321NCIndustry: Pharmaceuticals
Location: Basel und Region
Start: ASAP
Duration:
Workload: 100%
Introduction: Since its founding in 1997 ITech Consult AG has expanded its network of freelance IT continuously. Today we have access to over 30,000 reported IT specialists (developers, system specialists , project managers , supporters , etc. ) . So we are able to present computer science professionals with the required profiles in a short term.
Main Tasks:
-Participate in major cross-functional Electronic Document Management System (EDMS) project within Pharma Development, take active role on project delivery and success, collaborate with project team members and business SMEs across regions
-Ensure user requirements and technical solutions are aligned with the needs of the customer organizations
-Provide support for the business analysis work stream, from business process definition to detailed functional design
-Take responsibilities in functional design delivery
-Prepare, conduct and report meetings with SMEs (regular meetings and workshops)
-Communicate consistently with project team members and customers
Professional experience :
-5-8 years of business analysis experience in document management solution projects, Important is experience in clinical and regulatory projects.
-Experience with pharmaceutical industry, biotech, or other validated environment highly desired
-Experience as a consultant, functional expert, or similar role highly desirable
-Strong analytical skills, ability to learn new processes and new concepts, to link business processes with technical capabilities, to understand business concepts and system requirements
-Excellent written and oral communication skills in English; strong presentation skills
-Must be a self-starter, results-oriented and have a track record of timely, high-quality deliverables
-Must be a dynamic, pro-active and customer orientated contributor
-Proficient utilizing MS Office suite and other analytical tools
Important: Stakeholders are from different clinical, development and regulatory areas