Job Title : Validation Analyst, Clinical Systems
Location : Nottingham
Company : Worldwide Clinical Trials
Salary :
Open Date : 2024-03-07
Close Date : 2024-07-07
Who we are

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive

by being themselves and are inspired to do their best work every day. Join us

What Clinical Systems Validation Analyst does at Worldwide

To co-ordinate and perform validation and compliance activities for Worldwide's GxP systems.

What you will do
Author computer system validation documentation Catalogue and track project-specific validation documentation Tracking periodic review activities, including but not limited to disaster recovery and access reviews Responsible for collating and reporting metrics and preparing materials for Worldwide audits
What you will bring to the role
Ability to communicate concisely and effectively in both written and spoken English Problem Solving and Relationship Management skills Proficient in the use of common office software Self-motivated individual who can positively contribute to a team environment Ability to prioritize and handle multiple projects simultaneously Ability to demonstrate attention to detail
Your experience
Educated to degree level in a relevant discipline (Computing / Scientific) or able to demonstrate equivalent experience and at least 2 years’ experience within a computing, testing, scientific, quality or compliance environment. Experience of document authorship and control Experience of working within organizations employing GAMP, GxP, ISO standards. Ideally pharmaceutical industry, CRO, Clinical or Lab experience. Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations
We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at www.worldwide.com/careers For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .

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