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Job offers for Clinical Trials Monitor jobs in the United Kingdom

Top Job | Fulltime |

Enrollment, tracking study metrics, site management, vendor management, and Sponsor Oversight Visits, as requested. Works with Study Team (CRAs, CPMs, and Medical Monitors) to ensure successful planning, execution, and completion of clinical trials within expected timelines. Job responsibilities - Support

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Order to adjust tactical plans and be responsive to competitor activity. You will monitor customer complaints in conjunction with Business Unit Head Pharma ensuring appropriate and timely communication back to the customer. You will ensure close monitoring of supply and demand to meet customer

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Responsibilities Contribute to the clinical development strategy, including creating innovative strategies and clinical development plans to support global registration efforts and implementing operational plans for various malignancies. Serve as global medical monitor for one or more trials in

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21/04/2018 | Fulltime |

trials within a pharma/biotech/academic facilities - Protocol development experience - Vendor Management - Budget Management - Previous monitoring experience - Life Sciences Degree Keywords Clinical Project Manager, Clinical Trial Manager, Associate Clinical Trial Manager, Clinical Study Manager, London

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Identifying an investigational site and setting up, initiating, monitoring and closing down the ical trials may be carried out at various stages or phases and include trials on healthy humans, trials on patients with a disease, and studies conducted after the launch of a new drug to monitor safety

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Exposure - Reporting to the Clinical Risk Manager, you will be working cross functionally implementing global strategy at a local level - Responsible for monitoring your portfolio from clinical trial stage through post market studies and on-going usage maintaining safety standards and managing any risk

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Protocols - Responsible for the study budgets management - Responsible for the training of all site-monitors - Responsible for the overall management of site monitoring and associated documentation from study initiation through close-out to ensure compliance with regulatory requirements and Good Clinical

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Contract Clinical Operations Managers for international/global Oncology studies - Project and team oversight of Country Lead Monitors and outsourced monitoring activities - Key member of study project team in global pharma organisation, NO monitoring involved - 12 month extendable contracts

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At external clients (sponsors and investigator sites) Requirements Bachelor degree in a life - medical - natural sciences or scientific discipline or related area Minimum 3 years audit and GCP experience Experience in Clinical Quality Assurance and/or in Clinical Trials such as Monitoring or

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20/04/2018 | Fulltime

Clinical Trials Coordinator London, Immediate start We are looking for two full or part time Clinical Trial Coordinators to work with us, initially on a 6 month fixed term contract ( may be potential to extend) across a number of hospital sites in the London area. For the right candidate we can

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Study Lead Monitor role for global oncology studies with global pharma company - Key member of Study Team responsible for clinical operations, NO monitoring involved - Project team oversight of locally based Country Lead Monitors and outsourced CRO activities - Initial 12-month contract which

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19/04/2018 | Fulltime |

A nurse at Quotient your role is paramount to maintaining the safety of our volunteers in our 85 bed clinical unit in Ruddington. You will utilise nursing skills such as drug administration, venepuncture, cannulation, ECG, telemetry, vital sign monitoring and spirometry to assess the input of the

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Top Job | Fulltime

Clinical Operations Missions - Plan the clinical development program - Allocate appropriate resources for clinical studies - Supervise the smooth running of clinical trials and publications - Assist in the drafting and validation of clinical trial protocols - Manage, train and supervise the team of

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Contract Clinical Operations Managers for international/global Oncology studies - Project and team oversight of Country Lead Monitors and outsourced monitoring activities - Key member of study project team in global pharma organisation, NO monitoring involved - 12 month extendable contracts

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