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CTS Manager Maidenhead Very competitive salary Hybrid working 2x a week Initial 12 month contract which is likely to be extended This is an excellent opportunity for an experienced CTS Manager to join a global pharmaceutical company for an initial 12 months with the potential for this to be ...
This is an excellent opportunity for an experienced Clinical Trial Submissions Manager to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended
CTS Manager Maidenhead Very competitive salary Hybrid working 2x a week Initial 12 month contract ... Design and implement regulatory strategies and deliverables for global clinical trial applications ...
Clinical Trial Manager // Circulating Tumour Cell Diagnostics // Guildford You have dedicated your career to the design, set up, and execution of clinical studies. You have already helped oncology ...
A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical ...
You will be responsible for oversight of clinical trial protocols at a site level and will collaborate closely with he Clinical Trial Assistant (CTA, Trial Manager (TM) and Global Trial leader (GTL
Responsibilities: • Oversee a portfolio of CTAs, managing the preparation and dissemination of ... Minimum 2 years of CTA experience, with a preference for involvement in global clinical trial ...
Responsibilities: • Oversee a portfolio of CTAs, managing the preparation and dissemination of ... About You: * 2 years of CTA experience, with a preference for involvement in global clinical trial ...
Are you a Trial Master File expert looking for your next role? Then, Cencora Pharmalex is your ... Other clinical/document management systems * TMF stakeholders * End to end tasks, including TMF set ...
Represent area regulatory in clinical trial planning meetings and provide strategic and operational ... Experience of managing multi-national programmes of CTAs * Excellent understanding of the ...
Responsibilities Clinical Trial Conduct and Management: · Assist in the preparation of clinical trial documentation (e.g., regulatory submissions, study protocol update, IMPD amendment, etc.) · ...
Plan and manage regulatory submissions (e.g. clinical trial and marketing applications) in compliance with global filing plans and local regulatory requirements. * Implement product related ...
The role will work closely with UK Local Trial Managers and Site Managers (CRAs) to support inspection readiness across our clinical trial portfolio. The role also requires collaboration across other ...
You will act as the primary Data Management Lead for assigned projects, take responsibility for resourcing and planning and carry out leadership and management of projects and clinical trial data ...
Manage regulatory submissions (e.g. clinical trial and marketing applications) for products in compliance with global filing plans and local regulatory requirements. * Implement product related ...
Plan and manage regulatory submissions for clinical trial and marketing applications in compliance with global filing plans and local regulatory requirements. * Regulatory Strategy Implementation
Background in clinical trial management * Experience in Regulatory Affairs * Good level of knowledge of Clinical Trial Submissions on a local and regional level * Working knowledge of submissions ...
... clinical trial submissions managed by other stakeholders. § Ensure approved company CTA processes are followed within agreed timelines. § Review and maintain awareness of regulatory intelligence ...
You will manage a full portfolio of projects/studies across multiple therapeutic areas. You will ... Background in clinical trial protocol development * Excellent knowledge of the current market is ...
Biopharmaceutical industry experience and some knowledge and understanding of Clinical trial execution. * Budget and project management experience preferred. * Experience with Project Management ...
Risk management plans. * Safety development plan. * Clinical Trial Protocols. * Informed Consent Forms (ICF). * Safety Sections of Investigator's Brochure (IB) and IB addenda. * Clinical Study ...
... clinical trial submissions managed by other stakeholders such as IB, Protocols. * the approved company CTA processes are followed within agreed timelines. * understanding of CTR process and ...
... clinical trial submissions managed by other stakeholders such as IB, Protocols. • Ensuring the approved company CTA processes are followed within agreed timelines. • Good understanding of CTR ...