IQ
IQVIA
Gestern

Associate Manager or Manager, Clinical Operations(m/w/x)

Management
Vollzeit
Remote
Keine Angabe
Frankfurt am Main

In this role, you will lead a team in clinical operations, ensuring quality and efficiency in trial management. Your day-to-day responsibilities will include managing staff, overseeing training, and collaborating closely with a key pharmaceutical client to support impactful clinical projects.

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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
Bachelor-Abschluss

Berufserfahrung

6 Jahre

Deine 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

Tools & Technologien

ICH-GCPMicrosoft Office

Sprachen

Deutschverhandlungssicher

Englischverhandlungssicher

Deine Vorteile

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.

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