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Local Trial Manager(m/w/x)
Managing contracts and budgets for clinical trials at country level for a global CRO. 5+ years clinical research experience, 1-3 years local trial management, and Oncology expertise required. Direct country-level trial ownership.
Requirements
- Master’s or higher-level degree in life science
- Minimum of 5 years of clinical research experience in the pharmaceutical industry or CRO plus 1-3 years of local clinical trial management experience
- Therapeutic area expertise in Oncology
- Strong working knowledge of clinical research regulatory requirements, i.e., GCP and ICH guidelines
- Fluent language skills in German on at least C1 level and good command of English
- Strong IT skills in appropriate software and company systems
- Excellent decision-making and strong financial management skills
- Flexibility and ability to manage study teams in a virtual environment
- Willingness to travel occasionally for business meetings
Tasks
- Prepare high-level budget estimates for service requests
- Develop detailed budget proposals
- Manage contracts and review external service provider agreements
- Act as the primary contact for assigned trials at the country level
- Track project progress against planned timelines
- Monitor patient recruitment rates to meet enrollment targets
- Maintain and update trial management systems
- Analyze trial progress using management reports
- Participate in Health Authority inspections and internal audits
- Contribute to site-level recruitment strategies and contingency plans
- Manage vendor services and support vendor selection
- Review country-specific informed consent documents
- Ensure timely reporting of adverse events and serious adverse events
- Maintain accurate trial data and essential documents
- Collaborate with Global Trial Lead on quality issues
- Ensure accurate financial reporting and budget adherence
- Organize IEC/HA approvals to comply with local regulations
- Mentor or represent the functional area in process initiatives
Work Experience
- 5 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Advanced
Tools & Technologies
- GCP
- ICH
Not a perfect match?
- ICON plcFull-timeWith HomeofficeExperiencedFrankfurt am Main
- IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Mainfrom 70,100 / year - ICON plc
Local Trial Manager - FSP(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - 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
Local Trial Manager(m/w/x)
Managing contracts and budgets for clinical trials at country level for a global CRO. 5+ years clinical research experience, 1-3 years local trial management, and Oncology expertise required. Direct country-level trial ownership.
Requirements
- Master’s or higher-level degree in life science
- Minimum of 5 years of clinical research experience in the pharmaceutical industry or CRO plus 1-3 years of local clinical trial management experience
- Therapeutic area expertise in Oncology
- Strong working knowledge of clinical research regulatory requirements, i.e., GCP and ICH guidelines
- Fluent language skills in German on at least C1 level and good command of English
- Strong IT skills in appropriate software and company systems
- Excellent decision-making and strong financial management skills
- Flexibility and ability to manage study teams in a virtual environment
- Willingness to travel occasionally for business meetings
Tasks
- Prepare high-level budget estimates for service requests
- Develop detailed budget proposals
- Manage contracts and review external service provider agreements
- Act as the primary contact for assigned trials at the country level
- Track project progress against planned timelines
- Monitor patient recruitment rates to meet enrollment targets
- Maintain and update trial management systems
- Analyze trial progress using management reports
- Participate in Health Authority inspections and internal audits
- Contribute to site-level recruitment strategies and contingency plans
- Manage vendor services and support vendor selection
- Review country-specific informed consent documents
- Ensure timely reporting of adverse events and serious adverse events
- Maintain accurate trial data and essential documents
- Collaborate with Global Trial Lead on quality issues
- Ensure accurate financial reporting and budget adherence
- Organize IEC/HA approvals to comply with local regulations
- Mentor or represent the functional area in process initiatives
Work Experience
- 5 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Advanced
Tools & Technologies
- GCP
- ICH
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
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Mainfrom 70,100 / year - ICON plc
Local Trial Manager - FSP(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - 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