Clinical trial manager jobs in Guildford

Title: Clinical Trial Manager - Global Pharma - Complex Trials. We’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. Provides regional management of global PIb-III studies managed by Clinical Pr...

Represent area regulatory in clinical trial planning meetings and provide strategic and operational support for Company CTAs for Company sponsored clinical trial Primary interface to and from affiliate personnel in over 60 countries. Excellent understanding of the legislation governing the conduc...

We are seeking adventurous souls to join our team as a Clinical Trials Manager!. Experience the thrill of managing global clinical studies and shaping the future of medicine. Lead regional management efforts on Phase Ib-III clinical studies. Previous experience in clinical research or study manag...

Represent area regulatory in clinical trial planning meetings and provide strategic and operational support for Company CTAs for Company sponsored clinical trial Primary interface to and from affiliate personnel in over 60 countries. We’re currently recruiting for a Regulatory Clinical Trial Stra...

To perform the role of Clinical Trial Manager (CTM) on assigned trials on a 12 month contract. Accountable for the operational management of the local (UK & Ireland) component of a clinical trial. Leads local trial team to ensure integrity of trial conduct and assurance of patient safety. Require...

Previous clinical study management/clinical project management as a study manager/clinical project manager. ICON: Global Clinical Trial Manager ICON United Kingdom Remote. Collaborating with Regional Clinical Trial Manager to ensure country level study delivery aligned with global delivery plans....

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 ...

We're currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an ...

The CTOS is accountable for supporting the oversight of trial supplies, documentation, submissions, co-ordination of communication, and the management of complex technical systems to manage clinical ...

We are seeking adventurous souls to join our team as a Clinical Trials Manager! If you're passionate about making a difference in healthcare and thrive in dynamic environments, this is the ...

Clinical Trials Manager Duration: 12 month contract Location: Stockley Park (3 out of 5 days ... Interacts with cross-functional teams internally and externally to ensure trial progress. * Will ...

- Clinical Trials Manager * Virology, management of central lab * EMEA The CTM role will involve ... Interacts with cross-functional teams internally and externally to ensure trial progress

Their facility near Reading serves as the packaging and distribution hub for clinical trial ... They are now seeking an Office Manager to join their dynamic team. This position is a part-time ...

Lead the clinical trial team * Plan, deliver and manage clinical trial activities * Liaise with the clinical trial team members * Management of global vendors * Point of contact with sponsor on ...

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 ...

Life Sciences Recruitment is pleased to confirm that we are working with our global, fast-growing clinical trial supply (CTS) client, to hire a Project Manager to join their Unlicensed Medicines ...

Regulatory Affairs Associate The Regulatory Affairs Associate will be responsible for: • Managing the clinical trial applications in Europe and other selected countries • Keeping up to date with ...

Review of and input on documents related to clinical trial submissions managed by other stakeholders. * Ensure approved company CTA processes are followed within agreed timelines. * Review 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 ...

Lead projects, ensuring efficient project management, compliance, and high-quality deliverables. * Analyse phase III clinical trial data to support HTA submissions. * Provide statistical consultancy ...

... 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 ...

OFG are taking part in the 4-day working week trial! Job Title: Deputy Headteacher Location ... To work with the clinical team and monitor each individual student's Behaviour Support Plan ...

... clinically differentiated solutions that deliver measurably better patient outcomes and more ... Manage reprocessing of our Rental/Loan/Trial fleet of devices. * Assist with spare part warehouse ...