ICON plc
Clinical Trial Manager(m/w/x)
Full-timeWith HomeofficeExperienced
Frankfurt am Main
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IQIQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Frankfurt am Main
from 70,100 / year
Full-timeRemoteExperienced
Nejo AI Summary
Orchestrating local team activities, integrating across functions for study execution at a global research provider. Significant Early Phase clinical trial management exposure essential. Work within multidisciplinary international teams and strict regulatory environments.
Requirements
- Master’s or higher-level degree in life science
- At least 2 years of clinical trial management experience
- Significant exposure in managing Early Phase clinical trials
- Exceptional knowledge of clinical research regulatory requirements
- Excellent understanding of project financials and vendor management
- Effective communication skills and fluent in German and English
- High ability in abstract complex topics and strategic thinking
- High organizational and planning skills
- Excellent leadership and collaboration skills
- High degree of self-accountability and commitment
- Very good computer skills including Microsoft Word, Excel, PowerPoint
- Flexibility for occasional business travel
- Strong problem solving skills
- Ability to make decisions and drive results
Tasks
- Manage execution of clinical studies
- Orchestrate local trial team activities
- Integrate with other functions during trial phases
- Work within GCP and regulatory environments
- Collaborate with multidisciplinary international teams
- Lead local trial team in preparing trial documents
- Support investigative sites in contract and approval processes
- Ensure compliance with ICH-GCP and regulatory regulations
- Uphold ethical standards and patient safety
- Plan and conduct trials in line with regulatory requirements
- Set up and manage trial budgets
- Review budget updates based on trial changes
- Act as primary contact for vendors
- Manage vendor-related activities as per project needs
- Provide trial-specific training to internal and external partners
- Develop relationships with investigational sites
- Support CRAs in site communications
- Monitor compliance of trial sites with GCP and regulations
- Ensure adequate trial supply distribution to sites
- Oversee timely data entry and cleaning
- Facilitate on-time Data Base Lock
- Collect and archive required trial documents
- Identify risks and develop contingency plans
- Collaborate with project leader on problem-solving
- Report updates to Trial Leader
- Participate in quality and process improvement initiatives
Work Experience
- 2 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA RDS GmbH 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.
Not a perfect match?
- IQVIA RDS GmbH
Local Trial Manager(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Manager Clinical Operations, Single Sponsor(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main
IQIQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Frankfurt am Main
from 70,100 / year
Full-timeRemoteExperienced
Nejo AI Summary
Orchestrating local team activities, integrating across functions for study execution at a global research provider. Significant Early Phase clinical trial management exposure essential. Work within multidisciplinary international teams and strict regulatory environments.
Requirements
- Master’s or higher-level degree in life science
- At least 2 years of clinical trial management experience
- Significant exposure in managing Early Phase clinical trials
- Exceptional knowledge of clinical research regulatory requirements
- Excellent understanding of project financials and vendor management
- Effective communication skills and fluent in German and English
- High ability in abstract complex topics and strategic thinking
- High organizational and planning skills
- Excellent leadership and collaboration skills
- High degree of self-accountability and commitment
- Very good computer skills including Microsoft Word, Excel, PowerPoint
- Flexibility for occasional business travel
- Strong problem solving skills
- Ability to make decisions and drive results
Tasks
- Manage execution of clinical studies
- Orchestrate local trial team activities
- Integrate with other functions during trial phases
- Work within GCP and regulatory environments
- Collaborate with multidisciplinary international teams
- Lead local trial team in preparing trial documents
- Support investigative sites in contract and approval processes
- Ensure compliance with ICH-GCP and regulatory regulations
- Uphold ethical standards and patient safety
- Plan and conduct trials in line with regulatory requirements
- Set up and manage trial budgets
- Review budget updates based on trial changes
- Act as primary contact for vendors
- Manage vendor-related activities as per project needs
- Provide trial-specific training to internal and external partners
- Develop relationships with investigational sites
- Support CRAs in site communications
- Monitor compliance of trial sites with GCP and regulations
- Ensure adequate trial supply distribution to sites
- Oversee timely data entry and cleaning
- Facilitate on-time Data Base Lock
- Collect and archive required trial documents
- Identify risks and develop contingency plans
- Collaborate with project leader on problem-solving
- Report updates to Trial Leader
- Participate in quality and process improvement initiatives
Work Experience
- 2 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA RDS GmbH 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 RDS GmbH
Industry
Healthcare
Description
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
Not a perfect match?
- ICON plc
Clinical Trial Manager(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA RDS GmbH
Local Trial Manager(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Manager Clinical Operations, Single Sponsor(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main