Business Analyst (Basel, Health Authority, Biotech, Pharma, Regulatory Affairs, CSV, Clinical Development)

Kaiseraugst, Aargau  ‐ Vor Ort
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Beschreibung

We are currently looking for a Business Analyst in Kaiseraugst, Switzerland to join our team on client’s side. A great opportunity to work in an IT industry with exposure to new technologies and international environment. You will be part of a business analyst team working on the delivery of strategic projects to expand the functionality and user base of document management.


Major Accountabilities:

- Critically evaluate information gathered from multiple sources, reconciles conflicts, decomposes high-level information into details, abstracts up from low-level information to a general understanding, and distinguishes user requests from the underlying true needs
- Establish user requirements and functional requirements on the basis of identified business needs. This may include techniques such as using interviews, document analysis, requirements workshops, surveys, site visits, business process descriptions, use cases, and task/workflow analysis
- Serve as the conduit between the project managers and the software development team and Solution Architect through which requirements flow, including challenging project managers on their assumptions of how they will successfully execute their plans
- Take responsibility to ensure that the final solution matches the URS and meets the customers’ needs and support operational services teams in ensuring continued business value realization and business adoption
- Strive for very high quality standards of documentation and adherence to process.
- Connects with the Business Process Owner and business community bringing a value-adding Informatics point of view to help continuously improve business processes and solutions

Requirements:

- Several years’ of business analysis experience in multiple areas of business domain and technology or related field experience with Health Authority / Regulatory Authority
- Proficient knowledge of pharmaceutical Regulatory and Clinical processes, including knowledge and appreciation of scientific Regulatory affairs, ethical and compliance principles as well as Regulatory Affairs and/or Clinical Development experience
- Experience in document management solutions and preferably in performance optimization related projects
- Strong systems, user and functional requirements analysis and technical skills
- Proven skills in document authoring (e.g. User Requirements Specification, Functional Specifications) as well as in relationship building, customer-focus, decision-making and problem solving
- Excellent presentation, meeting facilitation and communications skills (written and verbal in English, other languages are plus)
- Formal training and proficiency in software development methodologies and computer systems validation in regulated industries (biotech/pharma)

We offer:

- Broad range of activities, tasks and projects
- Further development and professional advancement
- Friendly and international working environment
- Competitive salary and various benefits
Start
08.2019
Dauer
5 Monate
(Verlängerung möglich)
Von
D-ploy GmbH
Eingestellt
05.07.2019
Ansprechpartner:
Sarah Seglitz
Projekt-ID:
1793642
Vertragsart
Freiberuflich
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