Description
Clinical Research Associate (field based)
Job reference number: 14620
Location: Field based (M4 corridor)
Contract duration: 6 months
Remuneration: Competitive
Start date: ASAP
Description:
This is a field based role and candidate will be working in the South West and Midlands area, therefore being located along the M4 corridor would be ideal. We are looking for applicants with extensive proven monitoring experience across the life cycle of clinical trials and have experience in a range of therapeutic areas.
Key Accountabilities
- Proactive participation in the UK MC study team(s)
- Delivery of the study milestones, patient recruitment targets and data management activities at allocated centres, within the allocated resource/time/number of site visits.
- Collaboration with the Clinical Project Leader, Clinical Research Manager, other CRAs and the Study Delivery Associates to ensure that quality and quantity commitments are achieved in a timely and efficient manner
Key Responsibilities
- Execute allocated study work according to agreed study timelines, resources, recruitment, and budget, in agreement with Clinical Project Leader and Clinical Research Manager
- Contribute to the local clinical and operational feasibility assessments and site capability assessments and contribute to the selection of potential investigators.
- Provide input to the UK MC recruitment strategy for the allocated studies
- Effectively plan, conduct and complete site visits (site qualification, initiation, monitoring and close-out) providing timely and appropriately detailed reports and progress as necessary
- Support in the timely delivery of proper documents for submissions to EC/IRB, local Regulatory Authorities and Trusts, and accurate and timely payments to investigators
- Obtain and maintain essential documentation in compliance with ICH-GCP and local regulations both in the office and at site.
- Manage study supplies (ISF, CRF, etc), drug supplies and drug accountability at study sites.
- Drive patient recruitment in order to meet/exceed targets
- Monitor clinical study data for local and global clinical studies.
Deliver quality, compliance & governance standards
- Maintain knowledge of all clinical process and SOPs to ensure appropriate compliance to ICH-GCP/ABPI code of practice
- Ensure site compliance with GCP requirements including ISF documentation
- Comply with internal AstraZeneca clinical and marketing company governance guidelines
Please note that applicants must be able to demonstrate a valid right to work in the UK
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