Clinical Data Manager
Oxford Respiratory Trials Unit, Oxford Centre for Respiratory Medicine, Churchill Hospital, Experimental Medicine, Nuffield Department of Medicine (NDM) Oxford
Grade 6: £29,614 – £35,326 per annum (pro rata for part time)
We have an exciting opportunity for a Clinical Data Manager to join our growing clinical trials unit. The Oxford Respiratory Trials Unit specialises in the design, delivery and administration of trials across the field of Respiratory Medicine, as well as supporting trials led by other teams. Our scope of work includes clinical trials at all phases, including translational studies, phase II discovery studies and multicentre definitive randomised trials.
This post requires an analytical, proactive and motivated individual with experience of data management in a research context, and proven abilities in database design and testing, query management, and time management skills.
The Clinical Data Manager will perform a range of data-related activities across clinical trials and research projects run by the Oxford Respiratory Trials Unit (ORTU) and on behalf of external research groups – requiring data capture, storage, management, review and reporting. The postholder will be responsible for monitoring the completeness, accuracy, consistency and validity of trial data managed by ORTU, ensuring that datasets specified for each trial meet the standards of quality expected for reporting to regulatory bodies, especially the requirements of GCP, data protection and pharmacovigilance.
Reporting to the Lead for IT Systems and Data Management, and interacting with a multi-disciplinary team including Chief Investigators, the postholder will conduct the development of database and data capture solutions for upcoming studies and will be accountable for the oversight and timely delivery of clinical trial data and documentation according to agreed timelines and quality expectations. You must have strong organisational and time management skills, with the ability to independently manage conflicting priorities and meet tight deadlines. You will have excellent IT skills, proven attention to detail and the ability to identify and resolve issues as they arise. You must be able to interpret and process large amounts of complex information and be able to follow procedures. A thorough understanding of the regulatory environment surrounding clinical trials and prior experience with OpenClinica will be highly beneficial.
The post is full-time (part-time minimum of 30 hours per week will be considered) and fixed-term for 12 months in the first instance, with the possibility of further extension. Requests for an informal discussion should be sent to firstname.lastname@example.org.
Applications for this vacancy are to be made online. You will be required to upload a supporting statement and CV as part of your online application.
Only applications received before 12:00 midday on *03 February 2022*will be considered.
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