Data Analytics Operations Manager

Talentmark; Bracknell; On-site; GBP 65,000 - 83,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Talentmark is recruiting a Data Analytics Operations Manager for a global animal health company on a 12-month contract. The role is hybrid with two days per week on site in Bracknell.

You will lead risk assessment and reporting at the medicinal product level, using data from multiple sources to identify quality risks and guide mitigation with clinical trial teams across the product lifecycle.

Qualifications

• Degree in scientific subject or equivalent experience.
• Experience in GxP environment in pharma.
• Project management experience with quality risk management.
• Experience with clinical trials and clinical trial management.
• Leadership and strategic problem solving capabilities.

Responsibilities

• Lead risk assessment, review, control and reporting activities at the medicinal product level with key stakeholders in clinical trial teams.
• Utilise up-to-date data from multiple medicine sources to identify quality risks.
• Guide medicine business partners in developing mitigation plans to address identified risks.
• Responsible for reporting risk management information to key stakeholders throughout the product lifecycle.

Skills

Data analytics

Risk management

Leadership

Project management

Clinical trials

Quality processes

Education

Degree in a scientific subject

GxP environment experience

Job description

Talentmark are recruiting for a Data Analytics Operations Manager to join a global animal health company on a contract basis for 12 months. This is a hybrid role with 2 days per week on site in Bracknell.

Salary: £350 to £450 per day

Data Analytics Operations Manager Role:

• Lead risk assessment, review, control and reporting activities at the medicinal product level with key stakeholders in clinical trial teams
• Utilise up-to-date data from multiple medicine sources to identify quality risks
• Guide medicine business partners in developing mitigation plans to address identified risks
• Responsible for reporting risk management information to key stakeholders throughout the product lifecycle

Your Background:

• Hold a degree in a scientific subject or have equivalent working experience.
• Working experience in GxP environment 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.
• Demonstrated experience in leadership and strategic problem solving paired with good knowledge about processes and quality management.

Company:

Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one of the fastest growing animal health companies in the UK.

It is essential that applicants hold entitlement to work in the UK

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check