Applications are invited from suitably qualified candidates for a fixed-term contract position of 6 months initially as a Senior Clinical Trial Coordinator/Project Manager within a thriving Academic Research Organisation. The position may be extended with additional funding availability.
·Degree level qualification in a clinical or life sciences related subject.
·Minimum of six years’ experience gained working in clinical research or a closely related field e.g. Pharma or Medical Device sector. Relevant post-graduate research experience e.g. PhD may be taken into account if deemed applicable.
·Previous experience gained in a medical device clinical trial co-ordination unit (CRO or ARO) organisation delivering coordination services for device trials is required for this role with experience gained in any or all of the following: (a) clinical trial co-ordination/project or site management (b) clinical trial monitoring role (c) clinical trial data management role or (d) safety management.
· Experience in operational delivery of multisite studies.
·Experience working within a Quality Management adhering to QC and QA control systems and risk management processes.
·Experienced in leading and establishing new processes.
· Strong project management skills and ability to take the lead on the delivery of key project milestones.
· Leadership and mentoring skills.
·Excellent verbal and written communication/presentation skills.
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