Die KI-Suchmaschine für Jobs
Manager Clinical Operations, Single Sponsor(m/w/x)
Beschreibung
In this home-based role, you will lead a dedicated clinical team while managing the partnership with a key pharma client to ensure high-quality trial execution and staff development.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
6 Jahre
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
Tools & Technologien
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- •Attractive compensation
Betriebliche Altersvorsorge
- •Pension
Sonstige Vorteile
- •Accident insurance
- IQVIAVollzeitRemoteManagementFrankfurt am Main
- IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
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Senior CRA (Sponsor Dedicated)(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA RDS GmbH
Local Trial Manager(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Trial Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main
Manager Clinical Operations, Single Sponsor(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this home-based role, you will lead a dedicated clinical team while managing the partnership with a key pharma client to ensure high-quality trial execution and staff development.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
6 Jahre
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
Tools & Technologien
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
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.
- 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)
VollzeitRemoteBerufserfahrenab 70.100 / JahrFrankfurt am Main - ICON plc
Senior CRA (Sponsor Dedicated)(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA RDS GmbH
Local Trial Manager(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Trial Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main