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Senior Clinical Study Manager
View: 104
Update day: 01-06-2024
Location: Beverley Yorkshire and the Humber
Category: R & D IT - Software
Industry: Staffing Recruiting
Position: Mid-Senior level
Job type: Full-time
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Job content
CK Group have a fantastic opportunity for a Senior Clinical Study Manager to join an excellent multinational consumer goods company on an initial 10-month contract basis. You will be overseeing a pivotal medical device study taking place in Leeds. This is a remote position and you will only be required to attend the Leeds site on an ad-hoc basis. The Company: Founded in 1840, Our client is home to the world’s most trusted and best loved hygiene, health and nutrition brands. With this role, you’ll have the chance to make a real-world impact, developing products to improve the health of millions of people worldwide. The Role: responsibilities will include: Lead a local trial team to ensure integrity of trial conduct and assurance of patient safety Ensure that local/regional component of trial is planned, conducted, and reported in line with regulatory requirements Ensure that sponsored trials are conducted according to applicable regulations and SOPs/procedures to safeguard patient safety / wellbeing, and data integrity Deliver trial commitments, including quality, timeline, and budget. Your Background: To succeed in this role, you will: Have a Biological Science degree (and ideally additional clinical research certification) A proven track record of managing the entire clinical studies process in a pharmaceutical/medical device/consumer healthcare industry or at a CRO or clinical vendor. Have an in-depth and up to date knowledge of Good Clinical Practice and other regulatory standards (e.g. ISO 14155) -Excellent communication skills and ability to liaise with internal and external stakeholders. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 53919 in all correspondence.Loading ...
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Deadline: 16-07-2024
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