Fresenius Kabi Deutschland GmbH
Senior Manager Clinical Operations(m/w/x)
Full-timeOn-siteSenior
Bad Homburg vor der Höhe
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IQIQVIA
Sr Clinical Project Support Specialist - Sponsor dedicated(m/w/x)
Frankfurt am Main
from 58,500 / year
Full-timeOn-siteSenior
Nejo AI Summary
Supporting global clinical trials from planning to close-out, managing documentation and systems. Strong knowledge of GCP and ICH guidelines required. Work across rotating global sites, 5-person project teams.
Requirements
- University degree or comparable professional education
- Exceptional communication and stakeholder management skills
- Strong knowledge of GCP and ICH guidelines
- Excellent organizational and problem-solving skills
- Ability to work independently, prioritize tasks, and manage projects
- Experience in complex international environment
- Detail-oriented with strong commitment to quality and compliance
- Proficiency in MS Office and clinical trial systems/tools
- Fluent in written and spoken English
Tasks
- Support global clinical trials from planning to close-out
- Manage trial-related documentation and systems
- Ensure compliance with SOPs, ICH-GCP, and regulatory requirements
- Plan and coordinate trial activities across regions
- Maintain trial documentation (ISF, TMF, submissions)
- Collaborate with stakeholders, vendors, and trial teams
- Manage clinical trial systems and databases
- Prepare and distribute project plans and updates
- Monitor trial progress, budgets, and data
- Identify and implement corrective actions
- Coordinate documentation workflows and regulatory submissions
- Support trial close-out and deliverables preparation
- Coordinate logistics for trial meetings and supplies
- Contribute to quality oversight and best practices
- Act as a key point of contact for trial-related queries
Work Experience
- 5 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- MS Office
- clinical trial systems/tools
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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IQIQVIA
Sr Clinical Project Support Specialist - Sponsor dedicated(m/w/x)
Frankfurt am Main
from 58,500 / year
Full-timeOn-siteSenior
Nejo AI Summary
Supporting global clinical trials from planning to close-out, managing documentation and systems. Strong knowledge of GCP and ICH guidelines required. Work across rotating global sites, 5-person project teams.
Requirements
- University degree or comparable professional education
- Exceptional communication and stakeholder management skills
- Strong knowledge of GCP and ICH guidelines
- Excellent organizational and problem-solving skills
- Ability to work independently, prioritize tasks, and manage projects
- Experience in complex international environment
- Detail-oriented with strong commitment to quality and compliance
- Proficiency in MS Office and clinical trial systems/tools
- Fluent in written and spoken English
Tasks
- Support global clinical trials from planning to close-out
- Manage trial-related documentation and systems
- Ensure compliance with SOPs, ICH-GCP, and regulatory requirements
- Plan and coordinate trial activities across regions
- Maintain trial documentation (ISF, TMF, submissions)
- Collaborate with stakeholders, vendors, and trial teams
- Manage clinical trial systems and databases
- Prepare and distribute project plans and updates
- Monitor trial progress, budgets, and data
- Identify and implement corrective actions
- Coordinate documentation workflows and regulatory submissions
- Support trial close-out and deliverables preparation
- Coordinate logistics for trial meetings and supplies
- Contribute to quality oversight and best practices
- Act as a key point of contact for trial-related queries
Work Experience
- 5 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- MS Office
- clinical trial systems/tools
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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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?
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