Data Analytics Operations Manager

JR United Kingdom; Bracknell; On-site; GBP 45,000 - 70,000; Full time

Job summary

An established industry player is seeking a Data Analytics Operations Manager to lead Risk Management activities for Clinical Trials and Medicinal Product Lifecycle. This 12-month contract role offers the opportunity to utilize data to identify quality risks and guide business partners in developing mitigation plans. With a focus on leadership and strategic problem-solving, you will report clinical trial risk management information to key stakeholders, ensuring quality throughout the product lifecycle. Join a company recognized as a Top Employer in the UK, committed to fostering a diverse and inclusive culture while developing breakthrough therapies that improve lives.

Qualifications

• Master’s degree in a scientific discipline required.
• Experience in GxP within the pharmaceutical industry is essential.

Responsibilities

• Lead Risk Based Quality Management for Clinical Trials.
• Manage Risk Assessment and Reporting activities with stakeholders.

Skills

Leadership Skills

Strategic Problem-Solving

Quality Risk Management

Project Management

Organizational Skills

Data Analysis

Education

Master’s Degree in Scientific Discipline

Tools

MS Office

MS Project

Database Tools

Job description

Data Analytics Operations Manager, Bracknell

Client: [Client Name]

Location: Bracknell

Job Category: Other

EU work permit required: Yes

Job Views: 3

Posted: 28.04.2025

Expiry Date: 12.06.2025

Job Description:

Data Analytics Operations Manager - Product Development Quality Risk Management

12-month Contract

As a Data Analytics Operations Manager, you will lead Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle activities.

Tasks & Responsibilities:

• Lead Risk Based Quality Management for Clinical Trials in support of Medicinal Product Development and throughout the Product Lifecycle.
• Manage Risk Assessment, Review, Control, and Reporting activities with Key Stakeholders in Clinical Trial Teams and other partners.
• Utilize data from multiple sources to identify Quality Risks and assist Business Partners in this task.
• Guide Business Partners in developing mitigation plans and oversee their implementation.
• 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.
• Experience with clinical trials, clinical research, clinical trial management, or clinical auditing is a plus.
• Knowledge in Project Management and Quality Risk Management.
• Leadership and strategic problem-solving skills, with good process and quality management knowledge.
• Strong computer skills, including MS Office, MS Project, and database tools.
• Excellent organizational skills and ability to handle multiple tasks.
• Ability 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, committed to excellent HR policies and people practices. Learn more at: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work

About Us:

At Boehringer Ingelheim, we develop breakthrough therapies that improve lives. Founded in 1885, family-owned, with 52,000 employees worldwide, we foster a diverse, collaborative, and inclusive culture. We believe talented and passionate people can achieve great things.

Join us to grow, collaborate, innovate, and make a difference.

We offer a respectful, friendly global environment with a focus on learning and development. Boehringer Ingelheim is an equal opportunity employer committed to diversity and inclusion. Learn more at https://www.boehringer-ingelheim.com.