Expert Clinical Trials Data Management and Statistician (m/f/x) Bavaria
In this role you will be responsible for the development of the statistical section of clinical study protocols. Establishing a central database for clinical study data, define and programming. You design data entry systems (eCRF, eCOA, ePRO) for clinical studies and carry out user acceptance tests. Another big part of this position includes collection, cleaning and validating data.
Your responsibilities as ´Clinical Trials Data Manager and Statistician (m/f/x)´?
* You are responsible for the development of the statistical part of clinical study protocols.
* Together with the CROs, you define the strategy for the statistical analysis of clinical studies and review the statistical analysis plan (SAP)..
* Data collection, cleaning and validation are an integral part of your area.
* You carry out statistical analyses yourself and review the analyses of the CROs, interpret the results and present them to the team.
* You are involved in the preparation of clinical study reports (CSRs) and market approval dossiers.
* You design data entry systems (eCRF, eCOA, ePRO) for clinical studies and carry out user acceptance tests.
* You coordinate the selection of and collaboration with service providers (CROs) for data management and biostatistics and ensure that agreed quality standards and deadlines are met.
* You establish a central database for clinical study data and define and program relevant analyses and dashboards.
Your requirements as ´Plant Engineer DACH(m/f/x)´?
* You have completed an MS/MA degree or a PhD in biostatistics or similar and have at least 2 years of relevant work experience.
* You have previous experience in clinical research and in dealing with eCRF, eCOA, ePRO and clinical databases (e.g. Medidata).
* You have experience in coordinating service providers in the areas of data management and biostatistics.
* You are detail-oriented and analytical and have a precise, structured way of working.
* Fluent German and English skills You have hands-on expertise in programming data analyses in R or other relevant programming languages (e.g. Python, SAS).
Application process:-
CV to my email: c.quigg@sciproglobal.de-
Call with a presentation of the company-
I am your contact person for the entire application process (interviews to contract negotiations) i.e. You don't have to apply yourself-
Discuss other exclusive positions that are tailored to your profile
My contact details:E
mail : c.quigg@sciproglobal.deT
el: (direct dial) 089 2620 58 895L
inkedIn: https://www.linkedin.com/in/clodagh-quigg-b150b2200/
I look forward to your application!