i-Pharm Consulting

Regulatory Affairs - Data Reporting

Location
Frankfurt am Main
Salary
Negotiable
Posted
21 Nov 2018
Closes
17 Jan 2019
Ref
171118
Contract Type
Permanent
Regulatory Affairs - Data Reporting (m/f)

Frankfurt



We are looking for a Freelancer, expert in the development and analysis of reports, but also to provide experience in ​​the business, in this case, Regulatory Affairs.



Responsibilities



* Develop, implementation, maintenance and execution of regulatory data analysis reports.
* Conduct business analysis, collect business requirements and translate them into BI Solutions leveraging best practices.
* Maintenance and execution of existing data analysis reports.
* Data retrieval from the regulatory data management systems (RIMS) using SQL developer.
* Data Modelling in MS Excel (VBA) and data modelling tools like Business Objects, Oracle SQL developer.
* Run & create reports/analysis for assessments and on other kinds of data as required.
* Data mapping between RIMS and SAP.
* Developing and maintenance of processes & corresponding documentations for tracking and maintaining RIMS data reports.
* Developing, implementation, maintenance and execution of data quality reports from RIMS to prepare working packages for 1st level support on data cleansing.
* Utilize statistical data quality procedures or test-driven approach for quality assurance.
* Use strong analytical skills to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.
* Visualize and report insights creatively in a variety of formats to various stakeholders.



Requirements:



* Proven Experience as a Regulatory Affairs, assisting with the research, analysis and communication of information pertaining to the appropriate regulatory pathway for new or modified products.
* Proven and deep knowledge of MS Excel / SQL Developer and/or Business Objects.
* Good English & German Communication skills (verbal and writing).
* Proven Data Modelling experiences desired.
* Knowledge and proven experience about EU marketing authorization procedures desired.
* Knowledge about RIMS data models required.



To Apply:

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organizations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance, Information Technologies and Bioinformatics.

If you would like to discuss this vacancy further, please call Eloisa Reinoso on +49 (0) 8938035851, or email ereinoso@i-pharmconsulting.com. If this role is not suitable, but anyway you are looking for a job, it will be great to discuss other possible positions or answer any general questions regarding your career and the current market.

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