Associate business analyst - united kingdom, united kingdom

about us simbec-orion is a responsive and agile full-service cro, with wide therapeutic experience and specialist expertise in clinical pharmacology, oncology and rare diseases. perfectly structured, we provide full-service clinical development solutions for small and mid-size drug developers - headed up by a centralised leadership team. with a focus on tailormade and scalable solutions, we'll adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. because our goal is the same as theirs; to improve patients' lives. the role we are looking for an associate business analyst to join our business systems group where you will work with the support from more experienced business analyst to partner with a pre-defined business area of simbec-orion to work with our business and clinical users to support in driving business transformation by understanding the key business deliverables and what dependencies exist with other departments and the defined key inputs and outputs. you will work towards identifying opportunities for process improvement and prioritise the processes, which will return the greatest increase to productivity. you will identify and document all improvement requirements and manage the pre-project process and implementation of the solution. key accountabilities develop to-be process maps for assigned business area. develop ms project plans for assigned business area. creation of requirements specifications catalogue and project documentation. ensure solutions (comprising of technology, processes, people and data) work to deliver data security, accuracy, completeness, validity, timeliness and reliability. development of the change management strategy associated with a project, including training, role definitions, communications etc. ability to work with and co-ordinate with multiple vendors. create and execute installation qualification (iq), operation qualification (oq), performance qualification (pq) documents for gxp applications. collaborate with quality team to develop project validation documentation and test plans. executes protocols, performs testing sequences and change controls. administer enterprise applications and maintain (patch), repair and manage new and existing systems within a regulated environment. attend or provide support to external sponsor/regulatory audits and manage any audit responses. provide day to day and scheduled application support; respond to application support issues from multiple business customers. provide communications, both written and verbal, to the wider teams. skills required have a minimum of 1 year experience within a regulated industry or have a minimum of 2 years' experience outside of a regulated industry no project management experience would be required bcs training would be advantageous previous experience working within testing or validation teams would be an advantage why you should join us simbec-orion is growing fast. to keep up with demand, we're looking for the best people, from all areas of clinical development, to join our team. we're dedicated to bringing the latest advances in science to market. exposure to truly innovative new drugs in patient populations with serious unmet medical needs is what drives our company - and your reason to be a part of it. with experts from all disciplines under the same roof, you'll work alongside some of the industry's best. so if you'd like to further your career within challenging therapeutic areas in rare disease, oncology, or at our clinical pharmacology site, or laboratory services. we're waiting to hear from you. our clinical pharmacology site, or laboratory services. we're waiting to hear from you.

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