

Boehringer Ingelheim
Data Analytics Operations Manager
⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Data Analytics Operations Manager on a 12-month contract, requiring 2 days per week in Bracknell. Key skills include project management, leadership, and experience in GxP within the pharmaceutical industry. A Master's degree is required.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
Unknown
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🗓️ - Date
July 23, 2026
🕒 - Duration
More than 6 months
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🏝️ - Location
Hybrid
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📄 - Contract
Unknown
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🔒 - Security
Unknown
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📍 - Location detailed
Bracknell, England, United Kingdom
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🧠 - Skills detailed
#Project Management #Leadership
Role description
We are currently looking for a Data Analytics Operations Manager to join our Global Quality Medicine team on a contract basis for 12 months.
This role requires 2 days per week at Head office (Bracknell).
TASKS & RESPONSIBILITIES
• Imagine yourself at the heart of risk-based quality management for medicinal product development and throughout the product lifecycle.
• Picture yourself leading risk assessment, review, control and reporting activities at the medicinal product level with key stakeholders in clinical trial teams and other partners within and beyond Quality Medicine.
• Visualize utilizing up to date data from multiple medicine sources to identify quality risks. Your analytical skills will be crucial in assisting medicine business partners in this task.
• Envision yourself guiding medicine business partners in developing mitigation plans to address identified risks and ensuring implementation and oversight according to stakeholder agreements.
• Consider being responsible for reporting risk management information to key stakeholders throughout the product lifecycle.
REQUIREMENTS
• Masters degree in scientific discipline with a few years of experience in GxP within the pharmaceutical industry.
• Proven knowledge in project management including experience in quality risk management.
• Proficient experience with clinical trials, clinical research associate, clinical trial management or clinical auditing is considered a plus.
• Demonstrated experience in leadership and strategic problem solving paired with good knowledge about processes and quality management
• Strong computer skills including MS Office, MS Project, Database tools and the talent to quickly learn new systems.
• Excellent organizational skills and ability to accomplish multiple tasks of varied complexity simultaneously
• Outstanding capability and confidence to present complicated content in a clear understandable and targeted manner
• Top notch communication, interpersonal and negotiation skills, combined with fluency in English both spoken and written
We are currently looking for a Data Analytics Operations Manager to join our Global Quality Medicine team on a contract basis for 12 months.
This role requires 2 days per week at Head office (Bracknell).
TASKS & RESPONSIBILITIES
• Imagine yourself at the heart of risk-based quality management for medicinal product development and throughout the product lifecycle.
• Picture yourself leading risk assessment, review, control and reporting activities at the medicinal product level with key stakeholders in clinical trial teams and other partners within and beyond Quality Medicine.
• Visualize utilizing up to date data from multiple medicine sources to identify quality risks. Your analytical skills will be crucial in assisting medicine business partners in this task.
• Envision yourself guiding medicine business partners in developing mitigation plans to address identified risks and ensuring implementation and oversight according to stakeholder agreements.
• Consider being responsible for reporting risk management information to key stakeholders throughout the product lifecycle.
REQUIREMENTS
• Masters degree in scientific discipline with a few years of experience in GxP within the pharmaceutical industry.
• Proven knowledge in project management including experience in quality risk management.
• Proficient experience with clinical trials, clinical research associate, clinical trial management or clinical auditing is considered a plus.
• Demonstrated experience in leadership and strategic problem solving paired with good knowledge about processes and quality management
• Strong computer skills including MS Office, MS Project, Database tools and the talent to quickly learn new systems.
• Excellent organizational skills and ability to accomplish multiple tasks of varied complexity simultaneously
• Outstanding capability and confidence to present complicated content in a clear understandable and targeted manner
• Top notch communication, interpersonal and negotiation skills, combined with fluency in English both spoken and written






