IQVIA
Associate Manager or Manager, Clinical Operations(m/w/x)
Full-timeRemoteManagement
Frankfurt am Main
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ALAlimentiv
Clinical Operations Lead(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Overseeing clinical project compliance, training, and assessment visits for CRAs. Undergraduate degree and 7-9 years related experience required; Health Sciences, Life Sciences, or Nursing background preferred. Occasional site travel.
Requirements
- College diploma/degree
- 7-9 years related experience
- Undergraduate university degree (Bachelors or Honors Bachelors)
- 4-6 years' experience
- Health Sciences, Life Sciences or Nursing specialty preferred
- SoCRA and/or ACRP Certification/Designation
- Minimum of 3 years CRA experience
- Strong experience with EDC systems
- Proficiency with MS Office
- Strong written and verbal communication skills
- Highly effective interpersonal and organizational skills
- Proactivity
- Detail orientation
- Task-driven
- Highly organized
- Understanding of GCPs and local regulations
- Clinical monitoring knowledge
- Ability in report writing
- Strong understanding of clinical research documents
- Ability to handle multiple tasks
- Ability to meet deadlines in a dynamic environment
Tasks
- Oversee clinical operations for projects
- Ensure compliance with study protocols and regulations
- Act as a liaison between CRAs and the clinical project team
- Provide project-specific training for CRAs
- Conduct assessment visits with CRAs
- Implement enrollment and recruitment strategies
- Prepare monitoring plans and structural documentation
- Schedule monitoring visits and track performance metrics
- Manage issue escalation and corrective actions
- Develop study tools for site and CRA use
- Review visit reports for quality and compliance
- Track protocol deviations
- Support clinical operations objectives
- Monitor regional CRA compliance with study timelines
- Conduct co-monitoring visits as needed
- Assist in vendor management activities
- Proactively manage site and country performance
- Contribute to financial project management processes
- Manage investigator sites temporarily or permanently
- Conduct regular global CRA calls
- Attend meetings with Study Sponsor for status updates
- Provide operational support to the monitoring team
- Train and mentor regional CRAs on study procedures
- Serve as the first point of contact for CRAs
- Liaise with line managers for CRA assignments
- Conduct CRA assessment visits to evaluate performance
- Develop training materials and study tools
- Create and present materials for Sponsor meetings
Work Experience
- 3 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Bonus
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Alimentiv 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?
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Full-timeWith HomeofficeSeniorFrankfurt am Main
ALAlimentiv
Clinical Operations Lead(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Overseeing clinical project compliance, training, and assessment visits for CRAs. Undergraduate degree and 7-9 years related experience required; Health Sciences, Life Sciences, or Nursing background preferred. Occasional site travel.
Requirements
- College diploma/degree
- 7-9 years related experience
- Undergraduate university degree (Bachelors or Honors Bachelors)
- 4-6 years' experience
- Health Sciences, Life Sciences or Nursing specialty preferred
- SoCRA and/or ACRP Certification/Designation
- Minimum of 3 years CRA experience
- Strong experience with EDC systems
- Proficiency with MS Office
- Strong written and verbal communication skills
- Highly effective interpersonal and organizational skills
- Proactivity
- Detail orientation
- Task-driven
- Highly organized
- Understanding of GCPs and local regulations
- Clinical monitoring knowledge
- Ability in report writing
- Strong understanding of clinical research documents
- Ability to handle multiple tasks
- Ability to meet deadlines in a dynamic environment
Tasks
- Oversee clinical operations for projects
- Ensure compliance with study protocols and regulations
- Act as a liaison between CRAs and the clinical project team
- Provide project-specific training for CRAs
- Conduct assessment visits with CRAs
- Implement enrollment and recruitment strategies
- Prepare monitoring plans and structural documentation
- Schedule monitoring visits and track performance metrics
- Manage issue escalation and corrective actions
- Develop study tools for site and CRA use
- Review visit reports for quality and compliance
- Track protocol deviations
- Support clinical operations objectives
- Monitor regional CRA compliance with study timelines
- Conduct co-monitoring visits as needed
- Assist in vendor management activities
- Proactively manage site and country performance
- Contribute to financial project management processes
- Manage investigator sites temporarily or permanently
- Conduct regular global CRA calls
- Attend meetings with Study Sponsor for status updates
- Provide operational support to the monitoring team
- Train and mentor regional CRAs on study procedures
- Serve as the first point of contact for CRAs
- Liaise with line managers for CRA assignments
- Conduct CRA assessment visits to evaluate performance
- Develop training materials and study tools
- Create and present materials for Sponsor meetings
Work Experience
- 3 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Bonus
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Alimentiv 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
Associate Manager or Manager, Clinical Operations(m/w/x)
Full-timeRemoteManagementFrankfurt am Main - IQVIA
Manager Clinical Operations, Single Sponsor(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main - ICON plc
Clinical Site Manager(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main - ICON plc
Clinical Research Lead Assistant(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main - ICON plc
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main