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You will lead the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, including designing clinical studies and managing regulatory interactions. Additionally, you will collaborate with cross-functional teams to solve drug development challenges using modeling and simulation.
The clinician will perform comprehensive diagnostic assessments and provide patient visits while maintaining up-to-date treatment plans. They will also complete progress notes and collaborate with case management and psychiatric teams to ensure optimal client outcomes.
The Clinical Data Manager oversees the data management lifecycle for clinical trials, ensuring high-quality data collection and adherence to regulatory standards. They act as the primary data representative on project teams, managing study documentation, metrics, and cross-functional communication.
The Senior Clinical Data Coordinator manages clinical trial data activities, including ongoing data review and reconciliation of third-party and safety data. They are also responsible for performing User Acceptance Testing (UAT) and Quality Control (QC) on clinical databases to ensure high-quality deliverables.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately and on time. Responsibilities include managing system access, maintaining project documentation, and performing quality audits on trial files.
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The Director drives strategic and operational excellence across healthcare quality programs, clinical data systems, and contact center operations. They are responsible for leading high-performing teams to improve clinical outcomes, close care gaps, and manage complex client partnerships.
The Client Experience Manager will support pharmacy benefit plan changes, facilitate ID card processes, and manage reporting and invoicing. They will also oversee member support tasks, including prior authorization, claims resolution, and eligibility management.
The nurse will deliver cancer awareness roadshows and health promotion activities to community groups across the North West of England. They are also responsible for managing volunteers, collecting engagement data, and providing information on cancer prevention and early detection.
The role involves delivering face-to-face cancer prevention and early detection information to the public in various community and workplace settings. You will be responsible for engaging hard-to-reach audiences, collecting evaluation data, and representing the organization professionally.
Deliver the Cancer Awareness Roadshow and health promotion activities to engage communities in cancer prevention and early detection. Manage health awareness volunteers and collect data to evaluate the impact of local engagement activities.
Deliver face-to-face cancer prevention and early detection information to the public in various community and workplace settings. Collect and input data for evaluation purposes while representing the organization professionally.
Provide expert clinical consultation, teaching, and technical support for vascular medical devices within clinical settings. Maintain up-to-date knowledge of therapies and technologies while supporting the salesforce and conducting product presentations.
The associate will track rater experience qualification data and coordinate logistical matters for investigator meetings. They are also responsible for managing scale licenses, translations, and ensuring adherence to rater training and data surveillance plans.
The role involves designing specialty pharmacy networks, developing reimbursement models, and implementing cost-reduction strategies to meet affordability goals. The advisor will also analyze market trends and collaborate with internal and external stakeholders to optimize network performance.
The Senior Clinical Pharmacologist will lead clinical pharmacology strategies across early and late-phase drug development programs while partnering with cross-functional teams to drive decision-making. They will apply model-informed drug development principles to support dose selection, biomarker optimization, and regulatory submissions.
Lead a team of clinical professionals to deliver exceptional patient care within NHS-funded pathways while driving operational excellence. Own key performance metrics and strategic objectives to ensure the successful delivery and continuous improvement of clinical services.
The consultant will manage a portfolio of clients by providing practical health and safety advice and ensuring contractual compliance. They will also work closely with the Client Experience team to schedule visits and maintain strong, trusted client relationships.
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Provide technical support for DBS and SCS procedures in clinical settings and manage regional customer education. Develop and maintain professional relationships with hospital accounts while supporting the regional business strategy.
The Clinical Research Associate executes clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They are responsible for managing site performance, ensuring data quality, and collaborating with the Regional Clinical Operations Manager to meet study timelines.
Provide high-quality therapeutic care and comprehensive assessments through face-to-face, telephone, or video consultations. Collaborate with clinical leads and the therapy team to ensure evidence-based interventions and effective case management.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They ensure subject safety, data integrity, and proper management of investigational products while maintaining accurate site documentation.
The Clinical Success Manager will own and develop installed base accounts, serving as the primary point of contact to ensure customer satisfaction and long-term success. They will also drive revenue growth through upgrades and service offerings while acting as a bridge between customers and internal clinical and technical teams.
The On-Call Coordinator acts as the primary point of contact for clients and staff outside of office hours to manage schedules, staff absences, and emergency cover. They are responsible for providing support to Healthcare Assistants, ensuring service delivery, and documenting all incidents and communications accurately.
You will manage the operational aspects of clinical trials from initiation to close-out while ensuring compliance with regulatory standards and GCP. Additionally, you will lead and support cross-functional teams to deliver quality outcomes within established timelines and budgets.
The post-holder will review consultant prescribing recommendations and perform clinical pharmacy checks to ensure safe medication delivery. They will also counsel patients via telephone and manage prescribing across various specialties using remote software.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects and caregivers. They will also provide central monitoring by reviewing neuropsychological test data to ensure accuracy and provide feedback to other raters.
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The Clinical Development Manager will lead the launch and adoption of pulsed field ablation technologies across the south of the UK. They are responsible for managing a team of four specialists, building clinical advocacy, and ensuring site readiness for new product introductions.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects. They are also responsible for scoring assessments and providing central monitoring of neuropsychological test data to ensure accuracy.
Lead complex clinical trial projects and regulatory submissions while providing expert biostatistical guidance to sponsors. Collaborate with cross-functional teams to develop statistical analysis plans, review protocols, and ensure high-quality data deliverables.
The Senior Clinical Research Associate is responsible for ensuring data integrity, quality, and compliance with ICH GCP and protocol requirements at investigator sites. They will conduct monitoring activities, manage site-level performance, and coordinate with investigators to ensure trials are inspection-ready.
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