IQVIA
Manager Clinical Operations, Single Sponsor(m/w/x)
VollzeitRemoteSenior
Frankfurt am Main
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IQIQVIA
Associate Manager or Manager, Clinical Operations(m/w/x)
Frankfurt am Main
VollzeitRemoteManagement
Nejo KI-Zusammenfassung
Directing staff work and resolving employee relations for clinical research projects at a human data science company. 6+ years clinical research and line management experience, C1 German fluency required. Work focused on human data science for patient solutions.
Anforderungen
- Bachelor’s or higher-level degree in life science
- At least 6 years clinical research experience, including CRA experience
- Experience in a line management role or mandatory experience in a line management secondment for at least 6 months
- Fluent language skills in German on at least C1 level and good command of English
- Full knowledge of drug development process
- Full knowledge of applicable regulatory requirements, like ICH-GCP
- Strong knowledge of financial management and resourcing
- Strong knowledge of Microsoft Office applications
- Effective communication, organizational, interpersonal, teamwork and leadership skills
- Ability to independently coordinate and manage new processes and to effectively prioritize tasks
- Positive attitude and ability to interact with all levels of staff and ability to lead and motivate teams
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
- Flexibility to business travel and driving license
Aufgaben
- Manage staff according to organizational policies and regulations
- Plan, assign, and direct work for team members
- Assess performance and guide professional development
- Reward and discipline employees as necessary
- Address employee relations issues and resolve problems
- Participate in the hiring process by reviewing candidates and conducting interviews
- Ensure proper onboarding and training for new employees
- Provide staff with necessary materials, systems access, and training
- Oversee execution of training plans and SOP reviews
- Allocate resources to clinical research projects based on staff experience
- Manage quality of clinical work through regular reviews and evaluations
- Identify quality risks and create corrective action plans
- Ensure staff meet workload and quality metrics through regular reporting
- Support experienced managers in project reviews and analyses
- Assist with forecasting requirements and month-end activities
- Collaborate with customer counterparts on projects
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
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- 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 - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main
IQIQVIA
Associate Manager or Manager, Clinical Operations(m/w/x)
Frankfurt am Main
VollzeitRemoteManagement
Nejo KI-Zusammenfassung
Directing staff work and resolving employee relations for clinical research projects at a human data science company. 6+ years clinical research and line management experience, C1 German fluency required. Work focused on human data science for patient solutions.
Anforderungen
- Bachelor’s or higher-level degree in life science
- At least 6 years clinical research experience, including CRA experience
- Experience in a line management role or mandatory experience in a line management secondment for at least 6 months
- Fluent language skills in German on at least C1 level and good command of English
- Full knowledge of drug development process
- Full knowledge of applicable regulatory requirements, like ICH-GCP
- Strong knowledge of financial management and resourcing
- Strong knowledge of Microsoft Office applications
- Effective communication, organizational, interpersonal, teamwork and leadership skills
- Ability to independently coordinate and manage new processes and to effectively prioritize tasks
- Positive attitude and ability to interact with all levels of staff and ability to lead and motivate teams
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
- Flexibility to business travel and driving license
Aufgaben
- Manage staff according to organizational policies and regulations
- Plan, assign, and direct work for team members
- Assess performance and guide professional development
- Reward and discipline employees as necessary
- Address employee relations issues and resolve problems
- Participate in the hiring process by reviewing candidates and conducting interviews
- Ensure proper onboarding and training for new employees
- Provide staff with necessary materials, systems access, and training
- Oversee execution of training plans and SOP reviews
- Allocate resources to clinical research projects based on staff experience
- Manage quality of clinical work through regular reviews and evaluations
- Identify quality risks and create corrective action plans
- Ensure staff meet workload and quality metrics through regular reporting
- Support experienced managers in project reviews and analyses
- Assist with forecasting requirements and month-end activities
- Collaborate with customer counterparts on projects
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
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
IQVIA
Branche
Healthcare
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
Manager Clinical Operations, Single Sponsor(m/w/x)
VollzeitRemoteSeniorFrankfurt 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 - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main