Data Analytics Operations Manager

ZipRecruiter; Bracknell; On-site; GBP 45,000 - 70,000; Full time

Job summary

An established industry player is seeking a Data Analytics Operations Manager to spearhead Risk Management activities for Clinical Trials and Medicinal Product Lifecycle. This pivotal role involves leading risk assessments, utilizing data to identify quality risks, and guiding business partners in developing effective mitigation plans. The successful candidate will thrive in a dynamic environment, leveraging strong leadership and communication skills to drive quality management. Join a company recognized as a Top Employer in the UK, where innovation and collaboration are at the forefront of improving lives through breakthrough therapies.

Qualifications

• Master’s degree in a scientific discipline with experience in GxP.
• Proficient in clinical trials and quality risk management.

Responsibilities

• Lead Risk Management activities for Clinical Trials and Product Lifecycle.
• Report risk management information to Key Stakeholders.

Skills

Leadership

Strategic Problem-Solving

Communication Skills

Quality Risk Management

Clinical Trials Experience

Education

Master’s Degree in Scientific Discipline

Tools

MS Office

MS Project

Database Tools

Job description

Job Description

Data Analytics Operations Manager - Product Development Quality Risk Management

12-month Contract

As a Data Analytics Operations Manager, you will act as an expert leading Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle activities.

Tasks & Responsibilities

1. Be at the heart of Risk Based Quality Management for Clinical Trials, supporting Medicinal Product Development and throughout the Product Lifecycle.
2. Lead Risk Assessment, Review, Control, and Reporting activities with Key Stakeholders in Clinical Trial Teams and other organizational partners.
3. Utilize up-to-date data from multiple sources to identify Quality Risks, assisting Business Partners with analytical insights.
4. Guide Business Partners in developing mitigation plans for identified risks, ensuring their implementation and oversight per Stakeholder agreements.
5. Report Clinical Trial risk management information to Key Stakeholders throughout the Product Lifecycle.

Requirements

• Master’s degree in a scientific discipline with experience in GxP within the pharmaceutical industry.
• Proficient experience with clinical trials, clinical research, clinical trial management, or clinical auditing is a plus.
• Knowledge of Project Management, including Quality Risk Management.
• Leadership and strategic problem-solving experience, with good understanding of processes and quality management.
• Strong computer skills, including MS Office, MS Project, database tools, and the ability to quickly learn new systems.
• Excellent organizational skills with the ability to handle multiple tasks of varied complexity.
• Outstanding communication skills to present complex content clearly and effectively.

Why This is a Great Place to Work

Boehringer Ingelheim has been recognized as a Top Employer in the UK. This certification affirms our commitment to excellent HR policies and practices. To learn more, visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work

Our Company

At Boehringer Ingelheim, we develop breakthrough therapies that improve lives. Founded in 1885 and family-owned, we have 52,000 employees worldwide who foster a diverse and inclusive culture. Talented and passionate people drive our innovation.

Why Boehringer Ingelheim?

Join us to grow, collaborate, innovate, and make a difference. We offer challenging work in a respectful, friendly environment that values learning and development. We are committed to diversity and inclusion, benefiting our employees, patients, and communities.

Learn more at https://www.boehringer-ingelheim.com