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International Medical Affairs Senior Manager, MSL & Expansion Markets
LONDON, UNITED KINGDOM
...as primary contact for investigators interested in developing and performing studies with the company's commercially available assays in breast cancer. Assist in R&D and investigator-initiated studies as appropriate. Lead national and regional Advisory Boards when external advice is needed...
Junior Insolvency Investigator
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
...for a Junior Insolvency Investigator to join their team. Griffins are a national firm of licensed insolvency practitioners, established over 40 years ago, with collectively hundreds of years' experience across all aspects of insolvency practice and law, both in the UK and across many global...
Senior Medical Director - CNS/Neurology - Europe - Home-based
LONDON, ENGLAND, UNITED KINGDOM
...Medical Affairs at investigator and project team meetings. Collaborate with Worldwide Business Development to review and develop proposals, assess feasibility, attend general capabilities, or bid defense meetings. Engage in company and department initiatives, contribute to and participate in...
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Junior Insolvency Investigator
LONDON, SOUTH EAST ENGLAND
...a b Junior Insolvency Investigator /b to join their team. /p p br /p p Griffins are a national firm of licensed insolvency practitioners, established over 40 years ago, with collectively hundreds of years' experience across all aspects of insolvency practice and law, both in the UK and...
Associate Director, GCP and GLP Quality Assurance Cambridge, MA, United States Posted on 08/11/[...]
£80 - 100
CAMBRIDGE
...CROs), and Investigator Sites ensuring that outsourced third parties (CROs and other GCP/GLP service providers) are compliant and prepared for potential Sponsor and Regulatory Inspections. You will ensure that the appropriate processes, systems, and activities are in place and...
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Associate Director, Clinical Pharmacology
SURREY, ENGLAND, UNITED KINGDOM
...lead preparation of the Investigator s Brochure and clinical study reports, CTD modules, answers to HA questions. Supervises study setup (in co-operation with Clinical Operations and other study team members review of Task orders and deliverables) and study execution (Kick-off meeting Site...
Head of Field Medical Affairs
LONDON, UNITED KINGDOM
...medical team Strong compliance culture and timely ABPI review and certifications for CSL Vifor therapy areas Demonstrated knowledge and expertise in TAs and products through KOL engagement, presentations, education and training Strong relationships with KOLs, enhancing scientific engagement...
Environmental Team Lead
SPROWSTON
...policy and legislation compliance to the team. &bull Coordinate the monitoring and review of environmental legislative changes and the potential impact on the business. &bull Undertake regular reviews of the performance of personnel and contractors with regard to meeting...
Clinical Research Physician
CANNOCK, ENGLAND, UNITED KINGDOM
...fulfil the role of Sub-Investigator and Principal Investigator in clinical research studies in compliance with the protocol and ICH/GCP. KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED: Full and current GMC registration (essential) 4 years post-graduation experience (desirable) MRCP /MRCGP...
CRA II/ SCRA - Fast career development
CITY OF LONDON, ENGLAND, UNITED KINGDOM
...protocol and regulatory compliance and manages required documentation.. Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data...
QSHE Interface Lead
, , UNITED KINGDOM
...ensuring operational compliance with our SEMS and all relevant statutory provisions, codes and standards and good practice. This position is based in Norwich on a Monday to Friday basis however the position extends to cover the activities being undertaken on offshore assets and onshore...
Senior Manager, Quality
ABINGTON PIGOTTS, ENGLAND, UNITED KINGDOM
...programs, ensuring compliance with applicable ICH GCP and GLP standards and global regulations. As an integral member of the team tasked with product development, the position serves as a Quality and compliance business partner, engaging with multiple collaborators. The ideal candidate must...
Associate Clinical Project Manager
, , UNITED KINGDOM
...expectations and in compliance with IXICO quality and regulatory requirements. Act as the main point of contact for sponsors, 3rd party vendors and sites as applicable on assigned projects, depending on the level of their experience. Participate and provide updates during project team...
Senior Clinical Trial Manager
, , UNITED KINGDOM
Role Overview The Senior Clinical Trial Manager works within the clinical trial team to provide regional trial oversight and ensures deliverables are met in terms of quality, compliance, and timing. Strong vendor management is critical for this role. The position will report to the Director...
Clinical Project Manager
GREATER LONDON, ENGLAND, UNITED KINGDOM
...of presentations for investigator meetings and kick off meetings, as necessary. Coordinating cross functional teams, including external 3rd parties/vendors when necessary, to ensure efficient delivery of all project requirements. Provide project updates to clients on a regular basis, including...
Research Manager
CAMBRIDGE, ENGLAND, UNITED KINGDOM
...and budgets, ensuring compliance with study protocols, applicable laws and regulations (eg. ICH-GCP, the GDPR, where relevant), and with Omnigen standard operating procedures and associated documents. We have opportunities to work across various regions including the UK and South Africa. This is...
Head of Nonclinical Safety
UNITED KINGDOM, , UNITED KINGDOM
...merit and regulatory compliance. This hire will be the interface with health authorities acting as the company toxicology representative and addresses questions in interactions with FDA, EMA and other authorities on nonclinical safety topics. Responsibilities include: Responsible for developing...
Risk Based Quality Manager
NOTTINGHAMSHIRE, ENGLAND, UNITED KINGDOM
...activities and/or investigator sites potentially requiring sponsor intervention. Support Clinical Study Teams in understanding the impact, criticality and potential root causes of the findings and defining appropriate follow-up actions. Contribute and participate to the ongoing...
Clinical Quality Manager
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
...questions with the lead investigator, and writing reports Deliver mentoring and training within the organisation regarding the principles of effective clinical governance and ongoing improvement Provide cross cover and support as needed for other members ofthe Governance Team as necessary...
Clinical Study Lead (maternity leave)
UNITED KINGDOM, , UNITED KINGDOM
...including protocols, investigator brochure, informed consent, contracts, and reports, in compliance with relevant regulations, guidelines and SOPs. The Trial Lead is responsible for creating and implementing study-specific clinical monitoring tools and documents responsible for managing and...
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