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Full timeHealthcare

Team Lead, Clinical Trial Materials (m/f/d)

Randstad DeutschlandKöln, Nordrhein-Westfalen🇩🇪Germany

Why this role stands out

Step into a pivotal leadership role where you will accelerate your career by managing life-changing pharmaceutical projects within a supportive, globally recognized environment. You will thrive here if you are a collaborative mentor with a passion for operational excellence and a drive to guide teams toward high-impact results. With competitive compensation and comprehensive benefits, this is the perfect opportunity to advance your professional journey—apply online today to make your mark.

Quick overview

SeniorityMid Senior
Employment typeFull Time
Work modeOn Site
LocationKöln, Nordrhein-Westfalen, Germany

Job description

Are you an experienced professional looking to advance your career in a dynamic, global scientific environment? We are seeking a dedicated leader to join our customer's team in Cologne. At Randstad, we prioritize your professional growth, offering you a supportive work environment and the chance to contribute to the development of life-changing pharmaceutical innovations. We highly value diversity and warmly welcome applications from individuals with disabilities. Take the next step in your career and apply online today.

  • Guidance of operational team members and prioritization of daily shopfloor tasks
  • Coordinate workflow, staffing deployment, and assignments for operational continuity
  • Mentoring of team members through training, coaching, and competency development
  • Monitoring of daily production for adherence to quality, safety, and protocol standards
  • Facilitation of morning huddles and maintenance of operational status reporting
  • Management of material handling, inventory integrity, and expiration tracking
  • Support of audit readiness and participation in quality and regulatory inspections
  • Collaboration with cross-functional departments including logistics, IT, and quality assurance
  • Bachelor's degree in a relevant field or equivalent educational background
  • Minimum of one year of experience within the pharmaceutical industry
  • Demonstrated experience in clinical trial materials management
  • Proven proficiency in technical and administrative clinical trial documentation
  • Excellent English language skills for professional communication
  • Strong organizational and interpersonal abilities to manage team workflows
  • Adaptability to shifting project needs and high-pressure operational environments
  • Attractive pay according to the DGB/GVP collective agreement
  • Extensive social benefits, including holiday and Christmas bonuses
  • Up to 30 days of vacation time per year
  • Comprehensive and appreciative support throughout the entire application process
  • Access to a wide range of employee perks and discounts
  • Clear pathways for professional development and career progression

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