Clinical Trial Management Systems (CTMS) Specialist (hybrid)

Hobson Prior are currently looking for a Clinical Trial Management Systems (CTMS) Specialist to join a brilliant CRO on a permanent basis located in Letchworth Garden. The client is focused on offering exclusive, flawless approaches to bring transformative remedies to patients.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• Develop, author and publish training materials, such as training guides, user manuals and process flow maps. You will deliver training as needed.
• You will assess and implement User Acceptance Test scripts.
• Answer to department requests for practical support within CTMS system.
• For the role of Clinical Trial Management Systems (CTMS) Specialist, you will be responsible for delivering Subject Matter Expertise to the Clinical Systems Manager, project teams and other groups to guarantee effective set up, execution and maintenance of the Bionical Emas CTMS.
• Assist project teams with ad-hoc system support for their project specific configuration.
• The ideal candidate will be accountable for classifying gaps and/or areas for improvement in systems and processes.
• Any other practical task as permitted by your Line Manager.

Requirements:

• Educated to a University degree level or attained a suitable level of experience, a health care professional is ideal.
• Applicable clinical research experience (CRA, CTA, or other clinical research-related role) within the Pharmaceutical, Research or CRO industry.
• Ideally, you will have had preceding CTMS experience or other clinical program management system(s) experience.
• Strong understanding the Principles of Good Clinical Practice (GCP) and able to exhibit hands-on application.
• Solid knowledge of the drug development process, clinical study phases, have a capable level of clinical research literacy and medical terminology.
• Sophisticated language skills proven ability to communicate efficiently in a variety of electronic and face-to-face settings.
• A highly motivated individual who has a proactive approach to tasks.
• Functioning knowledge of ICH-GCP procedures and major Health Authority protocols as they pertain to the operational aspects of clinical studies and the management of TMF content.
• Demonstrated ability to co-operate in a team setting and work independently.
• Familiarity with software systems (EDC, CTMS, eTMF, IXRS) is an advantage, but not essential for the role.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.