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Senior Clinical Project Manager
We have a current opportunity for a Senior Clinical Project Manager working with IVDs on a contract basis. 6 months contract (possible extension) Clinical protocols, risk management plans, knowledge of IVD regulation within EuropeClient-facing position (face-to-face)Remote with occasional site visitsMonday - Friday, 39 hours per weekIf you are inte...
Regulatory / Medical Writer
We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.
Regulatory Affairs Specialist IVDR
We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested:6-12 months projectFull time (39 hours per week)HybridStart - May/JuneIVDR Regulatory Knowledge, getting ready for clinical trials.GAP AssessmentsTechnical DocumentsIVDR submissi...
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Regulatory Affairs Specialist IVDR
We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested:6-12 months projectFull time (39 hours per week)HybridStart - May/JuneIVDR Regulatory Knowledge, getting ready for clinical trials.GAP AssessmentsTechnical DocumentsIVDR submissi...
Clinical Data Associate
ABOUT THE COMPANYA global speciality pharmaceutical group focused on developing and commercialising treatments for patients with genetic, metabolic, systemic, and life-threatening acute disorders, as well as healthcare solutions for the general population. DESCRIPTION OF THE ROLEBased in Egham, Surrey, the Clinical Data Associate is expected to:Rev...
Regulatory Affairs Specialist IVDR
We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested:6-12 months projectFull time (39 hours per week)HybridStart - May/JuneIVDR Regulatory Knowledge, getting ready for clinical trials.GAP AssessmentsTechnical DocumentsIVDR submissi...