530+ English-Speaking Jobs in Mommenheim

KI-Beschreibung

In this role, you lead efforts to optimize patient operations, ensuring efficient onboarding and training for sample collection centers while promoting collaboration among internal teams to enhance therapy delivery.

• •
  5+ years of relevant professional experience
• •
  Experience with individualized therapies
• •
  Understanding of clinical site onboarding process

Deine Vorteile

KI-Beschreibung

You oversee safety planning and reporting for clinical trials, ensuring compliance with regulations and quality standards while managing safety data collection and interpretation across cross-functional teams.

• •
  Minimum 3 years of experience in clinical research
• •
  Advanced Degree in life sciences
• •
  Strong knowledge of regulatory requirements

Deine Vorteile

KI-Beschreibung

You provide statistical expertise to clinical projects, working with various teams to ensure accurate analysis, maintain quality control, and support strategic development in biostatistics.

• •
  Minimum 5 years in the pharmaceutical industry
• •
  At least 3 years of leadership experience in statistics
• •
  Experience in planning and analyzing oncology trials

Deine Vorteile

KI-Beschreibung

You will work in various areas within Global Supply Animal Health on innovative projects while gaining international experience and mentorship. This role includes collaboration and skill development through training and networking.

• •
  Excellent master's degree or Diploma
• •
  Strong team and communication skills
• •
  Leadership role interest for future

Deine Vorteile

KI-Beschreibung

You oversee the coordination and analysis of financial reporting, working with various departments to ensure timely reports and improve performance across the organization.

• •
  Master’s degree in business or related field
• •
  Track record in finance management in Pharma/
  Biotech sector
• •
  Experience in financial reporting and business planning

Deine Vorteile

KI-Beschreibung

You coordinate clinical trial documents and support project training and meetings, ensuring compliance with regulations and promoting effective communication within the team.

• •
  Experience in clinical trials project planning
• •
  Knowledge of relevant legislation and guidelines
• •
  Project management skills including teamwork

Deine Vorteile

KI-Beschreibung

You help create and refine consulting offerings by researching industry trends and developing frameworks. Additionally, you collaborate with teams to craft client proposals and improve business strategies.

• •
  1–2+ years of experience in consulting
• •
  Strong analytical and structured problem-solving skills
• •
  High proficiency in PowerPoint

Deine Vorteile

KI-Beschreibung

You oversee the entire software development lifecycle, from application design to issue resolution, while collaborating with teams to ensure high-quality performance and the adoption of best practices.

• •
  5+ years of professional backend development experience
• •
  Profound knowledge in PHP or Python
• •
  In-depth understanding of message-based systems

Deine Vorteile

KI-Beschreibung

You manage and oversee initiatives across various areas, ensuring effective project governance while contributing to data analysis and solution development.

• •
  Several years experience with management consultancy
• •
  International work experience in healthcare
• •
  C1 level English proficiency

Deine Vorteile

KI-Beschreibung

This role involves overseeing clinical data management activities, collaborating with various teams to ensure compliance and quality, while also supporting talent development and promoting best practices throughout the drug development lifecycle.

• •
  12-15 years experience in pharmaceuticals
• •
  10 years working with clinical data
• •
  Solid understanding of FDA and EMA regulations

Deine Vorteile

KI-Beschreibung

You oversee global regulatory strategies for Mental Health and Eye Health projects, guiding compliance efforts and fostering team excellence while ensuring that regulatory considerations align with business objectives.

• •
  High level of education in pharmacy
• •
  In-depth knowledge of Regulatory Affairs
• •
  Proven track record in regulatory strategies

KI-Beschreibung

You manage cross-functional teams to execute clinical studies, ensuring that quality standards and timelines are met while coordinating vendor oversight and regulatory submissions.

• •
  Minimum of 3 years of experience in project management
• •
  Profound knowledge of ICH-GCP legislation
• •
  Very good English

Deine Vorteile