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Data Scientist – Oncology(m/w/x)
Overseeing multiple clinical studies for tailored healthcare software solutions, assessing design feasibility. 4 years clinical trials experience and OMOP CDM knowledge essential. Cross-functional collaboration with OMOP experts and clinicians.
Requirements
- MSc or equivalent in clinical, biomedical sciences, nursing
- Experience designing RWE studies
- OMOP CDM knowledge and vocabulary mapping processes
- 4 years of work experience including clinical trials experience
- Excellent knowledge of Medical Dictionaries for coding
- Strong communication and interpersonal skills
- Experience working with diverse scientific backgrounds
- Ability to manage multiple tasks under timelines
- Strong commitment to pragmatic innovation
- Operational knowledge of GDPR for medical research
- Knowledge of key issues in pharmaceutical and healthcare industries
- Fluency in English (spoken and written)
- PhD in relevant discipline
- Support data management and OMOP teams
- Technical proficiency in R and SQL
- Knowledge of open-source federation solutions
- Willingness and ability to travel
Tasks
- Oversee multiple oncology studies
- Collaborate with OMOP experts, statisticians, and medical writers
- Coordinate with clinicians, data managers, and data scientists
- Assess feasibility of study designs based on source data
- Plan and manage resources for study objectives
- Understand scientific study protocols related to oncology
- Develop study plans with tasks, responsibilities, and timelines
- Track progress and document risks with team members
- Design and deliver client reports and presentations
- Build long-lasting client relationships through regular contact
- Ensure timely abstract submission and high-impact publications
- Coordinate a team to develop new study delivery methods
- Lead high-impact publications and thought leadership in clinical informatics
- Support initiatives around real-world evidence strategy
- Provide guidance on real-world data landscape to junior colleagues
Work Experience
- 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- R
- SQL
- OMOP CDM
- GDPR
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Data Scientist – Oncology(m/w/x)
Overseeing multiple clinical studies for tailored healthcare software solutions, assessing design feasibility. 4 years clinical trials experience and OMOP CDM knowledge essential. Cross-functional collaboration with OMOP experts and clinicians.
Requirements
- MSc or equivalent in clinical, biomedical sciences, nursing
- Experience designing RWE studies
- OMOP CDM knowledge and vocabulary mapping processes
- 4 years of work experience including clinical trials experience
- Excellent knowledge of Medical Dictionaries for coding
- Strong communication and interpersonal skills
- Experience working with diverse scientific backgrounds
- Ability to manage multiple tasks under timelines
- Strong commitment to pragmatic innovation
- Operational knowledge of GDPR for medical research
- Knowledge of key issues in pharmaceutical and healthcare industries
- Fluency in English (spoken and written)
- PhD in relevant discipline
- Support data management and OMOP teams
- Technical proficiency in R and SQL
- Knowledge of open-source federation solutions
- Willingness and ability to travel
Tasks
- Oversee multiple oncology studies
- Collaborate with OMOP experts, statisticians, and medical writers
- Coordinate with clinicians, data managers, and data scientists
- Assess feasibility of study designs based on source data
- Plan and manage resources for study objectives
- Understand scientific study protocols related to oncology
- Develop study plans with tasks, responsibilities, and timelines
- Track progress and document risks with team members
- Design and deliver client reports and presentations
- Build long-lasting client relationships through regular contact
- Ensure timely abstract submission and high-impact publications
- Coordinate a team to develop new study delivery methods
- Lead high-impact publications and thought leadership in clinical informatics
- Support initiatives around real-world evidence strategy
- Provide guidance on real-world data landscape to junior colleagues
Work Experience
- 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- R
- SQL
- OMOP CDM
- GDPR
About the Company
IQVIA Commercial GmbH & Co. OHG
Industry
Healthcare
Description
The company specializes in tailored software solutions for the healthcare market and develops custom software for billing audits.
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