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Manager Clinical Operations, Single Sponsor(m/w/x)
Managing clinical operations staff, planning team workloads, and guiding professional development. Six years clinical research and CRA experience with line management background required. Dedicated client focus.
Anforderungen
- Bachelor’s or higher degree in life science
- Six years clinical research and CRA experience
- Line management role or mandatory secondment experience
- German C1 level and English proficiency
- Knowledge of drug development process
- Knowledge of regulatory requirements and ICH-GCP
- Knowledge of financial management and resourcing
- Knowledge of Microsoft Office applications
- Communication, organizational, interpersonal and leadership skills
- Independent process management and task prioritization
- Positive attitude and team motivation ability
- Effective working relationships with stakeholders
- Business travel flexibility and driving license
Aufgaben
- Manage staff according to company policies and regulations
- Plan, assign, and direct team workloads
- Assess performance and guide professional development
- Handle employee relations and resolve workplace problems
- Review candidates and conduct interviews for new hires
- Oversee employee onboarding and initial training
- Ensure staff have necessary materials and systems access
- Execute training plans and SOP reviews
- Allocate staff to clinical projects based on experience
- Evaluate the quality of clinical work products
- Identify quality risks and create corrective action plans
- Monitor workload and quality metrics through regular reporting
- Analyze project performance and financial variances
- Support forecasting requirements and month-end activities
- Implement process improvement initiatives and workstreams
- Collaborate closely with the customer's counterparts
Berufserfahrung
- 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- ICH-GCP
- Microsoft Office
Benefits
Attraktive Vergütung
- Attractive compensation
Betriebliche Altersvorsorge
- Pension
Sonstige Vorteile
- Accident insurance
Noch nicht perfekt?
- IQVIAVollzeitRemoteManagementFrankfurt am Main
- IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Mainab 70.100 / Jahr - ICON plc
Senior CRA (Sponsor Dedicated)(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Trial Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA RDS GmbH
Local Trial Manager(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main
Manager Clinical Operations, Single Sponsor(m/w/x)
Managing clinical operations staff, planning team workloads, and guiding professional development. Six years clinical research and CRA experience with line management background required. Dedicated client focus.
Anforderungen
- Bachelor’s or higher degree in life science
- Six years clinical research and CRA experience
- Line management role or mandatory secondment experience
- German C1 level and English proficiency
- Knowledge of drug development process
- Knowledge of regulatory requirements and ICH-GCP
- Knowledge of financial management and resourcing
- Knowledge of Microsoft Office applications
- Communication, organizational, interpersonal and leadership skills
- Independent process management and task prioritization
- Positive attitude and team motivation ability
- Effective working relationships with stakeholders
- Business travel flexibility and driving license
Aufgaben
- Manage staff according to company policies and regulations
- Plan, assign, and direct team workloads
- Assess performance and guide professional development
- Handle employee relations and resolve workplace problems
- Review candidates and conduct interviews for new hires
- Oversee employee onboarding and initial training
- Ensure staff have necessary materials and systems access
- Execute training plans and SOP reviews
- Allocate staff to clinical projects based on experience
- Evaluate the quality of clinical work products
- Identify quality risks and create corrective action plans
- Monitor workload and quality metrics through regular reporting
- Analyze project performance and financial variances
- Support forecasting requirements and month-end activities
- Implement process improvement initiatives and workstreams
- Collaborate closely with the customer's counterparts
Berufserfahrung
- 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- ICH-GCP
- Microsoft Office
Benefits
Attraktive Vergütung
- Attractive compensation
Betriebliche Altersvorsorge
- Pension
Sonstige Vorteile
- Accident insurance
Über das Unternehmen
IQVIA
Branche
Pharmaceuticals
Beschreibung
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Noch nicht perfekt?
- IQVIA
Associate Manager or Manager, Clinical Operations(m/w/x)
VollzeitRemoteManagementFrankfurt am Main - IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Mainab 70.100 / Jahr - ICON plc
Senior CRA (Sponsor Dedicated)(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Trial Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA RDS GmbH
Local Trial Manager(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main