Do you have experience in laboratory experience or do you have a science degree? What are you waiting for? We are hiring for a Clinical study coordinator
Role: Clinical study coordinator
Location: Witney
Salary: upto £15.38
Job Type: 12 months contract
Job Overview:
The Clinical Study Co-coordinator assists delivery of studies to support both product development, manufacturing and the post market surveillance program for all ADC products.
Roles & Responsibilities:
- Maintain, calibrate and use laboratory equipment; perform site visits when required to support sites / train on equipment
- Ensure adequate stock, accountability and shipment of study materials
- Provide assistance to CRAs in the preparation and maintenance of study documentation and files
- Facilitate archiving of in house study documentation
- Ensure studies are implemented successfully by maintaining effective communication with study centers, external partners (i.e. translators, printers, CROs etc.) and ADC internal groups
- Ensure clinical studies are conducted according to health and safety guidelines and study materials are disposed of appropriately
- Review clinical study requests, provide clinical input and liaise with project teams to ensure their clinical testing needs are met
- Identify and implement changes to clinical processes and procedural documentation
- Ensure all clinical studies meet internal / external standards and GCP requirements can be made
- Responsible for compliance with applicable corporate and divisional policies and performing other duties as assigned by management
Skills:
- Must be accurate and organized in work approach and have good attention to detail
- Good judgement and communication (written and oral) skills for interaction with study site personnel and external vendors
- Ability to priorities work in an environment of complex and conflicting inputs, be accurate and organized in work approach and have good attention to detail
- Have analytical skills able to digest information from clinical studies and report findings
- The above background prerequisites are required to ensure that the jobholder can effectively and confidently support clinical studies that meet laid procedural and regulatory requirements
If this sounds interesting to you, please apply with your updated CV & I will get in touch with you.
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
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