IQVIA
Principal Medical Writer – Clinical Pharmacology(m/w/x)
Full-timeOn-siteExperienced
Frankfurt am Main
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IQIQVIA
Associate Medical Director- Oncology ,Sponsor-Dedicated(m/w/x)
Frankfurt am Main
Full-timeOn-siteSenior
Nejo AI Summary
Managing medical content for oncology clinical trial protocols for life sciences clients. 5-7 years' clinical medicine experience and a medical degree required. Sponsor-dedicated role within clinical research services.
Requirements
- Medical degree from accredited, internationally recognized medical school
- Minimum 5-7 years' experience in clinical medicine
- Robust, current knowledge of scientific, clinical, regulatory, commercial, competitive landscape
- Knowledge of federal, local regulations, guidelines for clinical research
Tasks
- Serve as a core member of trial teams.
- Manage medical content in Clinical Trial Protocols.
- Collaborate with project, safety, writing, and trial teams.
- Provide medical input for CTP updates.
- Define medically critical data, processes, and risks.
- Contribute to the Integrated Quality and Risk Management Plan.
- Participate in risk discussions during trial conduct.
- Co-author the Clinical Quality Monitoring Plan.
- Align CQMP with IQRMP risks and mitigations.
- Provide medical input on important protocol deviations.
- Review and support decisions on iPDs.
- Address and communicate clinical quality issues.
- Contribute to preparing core trial documents and milestones.
- Design eCRFs and translate medical questions.
- Develop Information for CRF Completion (ICC).
- Develop Data Review Plans.
- Specify lab parameters.
- Contribute to Data Transfer Agreements and alerts.
- Manage medical content for patient information.
- Manage medical content for informed consent.
- Manage medical content for trial monitoring manuals.
- Manage medical content for communication and training plans.
- Manage medical content for statistical analysis plans.
- Contribute to patient narrative preparation.
- Plan and review medical sections of Clinical Trial Reports.
Work Experience
- 5 - 7 years
Education
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Clinical Lead, Early Clinical and Experimental Therapeutics(m/w/x)
Full-timeOn-siteJuniorFrankfurt am Main - IQVIA
Principal Statistical Programmer - FSP(m/w/x)
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IQIQVIA
Associate Medical Director- Oncology ,Sponsor-Dedicated(m/w/x)
Frankfurt am Main
Full-timeOn-siteSenior
Nejo AI Summary
Managing medical content for oncology clinical trial protocols for life sciences clients. 5-7 years' clinical medicine experience and a medical degree required. Sponsor-dedicated role within clinical research services.
Requirements
- Medical degree from accredited, internationally recognized medical school
- Minimum 5-7 years' experience in clinical medicine
- Robust, current knowledge of scientific, clinical, regulatory, commercial, competitive landscape
- Knowledge of federal, local regulations, guidelines for clinical research
Tasks
- Serve as a core member of trial teams.
- Manage medical content in Clinical Trial Protocols.
- Collaborate with project, safety, writing, and trial teams.
- Provide medical input for CTP updates.
- Define medically critical data, processes, and risks.
- Contribute to the Integrated Quality and Risk Management Plan.
- Participate in risk discussions during trial conduct.
- Co-author the Clinical Quality Monitoring Plan.
- Align CQMP with IQRMP risks and mitigations.
- Provide medical input on important protocol deviations.
- Review and support decisions on iPDs.
- Address and communicate clinical quality issues.
- Contribute to preparing core trial documents and milestones.
- Design eCRFs and translate medical questions.
- Develop Information for CRF Completion (ICC).
- Develop Data Review Plans.
- Specify lab parameters.
- Contribute to Data Transfer Agreements and alerts.
- Manage medical content for patient information.
- Manage medical content for informed consent.
- Manage medical content for trial monitoring manuals.
- Manage medical content for communication and training plans.
- Manage medical content for statistical analysis plans.
- Contribute to patient narrative preparation.
- Plan and review medical sections of Clinical Trial Reports.
Work Experience
- 5 - 7 years
Education
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Not a perfect match?
- IQVIA
Principal Medical Writer – Clinical Pharmacology(m/w/x)
Full-timeOn-siteExperiencedFrankfurt am Main - SUSONITY
(Sr.) Medical Science Liaison Rare Disease / Tumour(m/w/x)
Full-time/Part-timeOn-siteSeniorMünchen, Köln, Gießen, Mainz, Frankfurt am Main, Göttingen, Erfurt, Leipzig, Dresden - Scholar Rock
Country Medical Director(m/w/x)
Full-timeOn-siteSeniorFrankfurt am Main, München - Sanofi
Clinical Lead, Early Clinical and Experimental Therapeutics(m/w/x)
Full-timeOn-siteJuniorFrankfurt am Main - IQVIA
Principal Statistical Programmer - FSP(m/w/x)
Full-timeOn-siteSeniorFrankfurt am Main