Cerner Enviza
25.02.2024
München
in all of these, there has never been a better time to join us and make a difference to our clients and the lives of patients. Key Purpose: The Director of Clinical Data Management & Safety is responsible for managing the
Daiichi Sankyo Europe GmbH
26.02.2024
München
stakeholders • Support the incorporation of the developed PRO strategy into study operations by overviewing data collection and related processes • Manage vendors in the conduct of projects involving PROs • Support the
Daiichi Sankyo Europe GmbH
10.03.2024
München
stakeholders • Support the incorporation of the developed PRO strategy into study operations by overviewing data collection and related processes • Manage vendors in the conduct of projects involving PROs • Support the
Daiichi Sankyo Europe GmbH
19.03.2024
München
stakeholders • Support the incorporation of the developed PRO strategy into study operations by overviewing data collection and related processes • Manage vendors in the conduct of projects involving PROs • Support the
Daiichi Sankyo Europe GmbH
10.03.2024
München
implementation, and track-record of successful publications • Expertise in various RWD sources (EMR/EHR, claims, disease registries, etc.) and clinical data standards, as well as understanding of RWD landscape across various
Daiichi Sankyo Europe GmbH
27.02.2024
München
literature reviews to build payer evidence, economic models, and Global Value Dossiers Oversee analysis of clinical trial data for cost effectiveness models and market specific ad-hoc requests for reimbursement submissions
Daiichi Sankyo Europe GmbH
11.03.2024
München
literature reviews to build payer evidence, economic models, and Global Value Dossiers Oversee analysis of clinical trial data for cost effectiveness models and market specific ad-hoc requests for reimbursement submissions
Daiichi Sankyo Europe GmbH
19.03.2024
München
closely with the global HEOR Product Lead(s) and provides relevant input to ensure that clinical trials and global evidence generation programs deliver the data/evidence required for successful market access in the European
Daiichi Sankyo Europe GmbH
04.03.2024
München
review. Acts as main statistical contact for the assigned studies and projects. Provides guidance to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data. Work
Olink Proteomics
23.02.2024
München
their clinical questions related to understanding real-time biology, stratifying patients, and developing drugs. Check out our PEA technology here: https://www.olink.com/our-platform/our-pea-technology/ Primary
ITM Isotope Technologies Munich SE
10.03.2024
Garching, München
authorities, and advisory boards • Clinical Development Activities: Support Clinical Medical Lead(s) in study strategy, design, data analysis, interpretation, and report generation • Regulatory Contribution and Study Oversight
Daiichi Sankyo Europe GmbH
29.02.2024
München
aus dem deutschen Versorgungskontext zu gewinnen • Gap-Analyse des klinischen Studienprogramms und Ableitung von Maßnahmen, wie diese geschlossen werden können • Bewertung und Initiierung von Real World Data (RWD-)Projekten
Daiichi Sankyo Europe GmbH
10.03.2024
München
aus dem deutschen Versorgungskontext zu gewinnen • Gap-Analyse des klinischen Studienprogramms und Ableitung von Maßnahmen, wie diese geschlossen werden können • Bewertung und Initiierung von Real World Data (RWD-)Projekten
Daiichi Sankyo Europe GmbH
19.03.2024
München
aus dem deutschen Versorgungskontext zu gewinnen • Gap-Analyse des klinischen Studienprogramms und Ableitung von Maßnahmen, wie diese geschlossen werden können • Bewertung und Initiierung von Real World Data (RWD-)Projekten
iOmx Therapeutics AG
22.03.2024
Martinsried, Germering
. • Contributing to clinical development plans and study protocols from the operations perspective. • Acting as a key member of a cross-functional clinical development team (clinical operations, data management, safety reporting, etc
Daiichi Sankyo Europe GmbH
01.03.2024
München
media screening for own and competitor brands, using innovative tools • Classify medical-scientific publications and clinical trial information • In collaboration with Insights Director, co-manage cross-functional CI