Clinical trial manager jobs in Harrow

Proclinical are seeking a dedicated Snr Clinical Trial/ Program Manager to accelerate the initiation and execution of Advanced Therapy Medicinal Products (ATMPs) clinical trials within one of our ...

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 ...

- Role: Clinical Trial Assistant (CTA / Associate CPM) * Location: Hybrid (4 days remote and 1 day ... and management of vendor invoices and Purchase Orders (POs) * Involved in internal process ...

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 ...

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 ...

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 ...

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

Join a team dedicated to improving patient outcomes through the effective management of clinical trial data, having a direct positive impact on patients lives. * An excellent platform with the chance ...

You will be expected to take responsibility for overseeing clinical trial administrators and other project team members: delegating and managing their work and providing feedback to them and the Head ...

Ensuring global clinical trial material supply for assigned studies. * Facilitating timely startup of new studies through prompt supply availability. * Managing clinical packaging and distribution ...

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 ...

Ensuring global clinical trial material supply for assigned studies. * Facilitating timely startup of new studies through prompt supply availability. * Managing clinical packaging and distribution ...

Must have acquired a good understanding of clinical research phases and the processes involved in the planning and management of a clinical trial. * Experience of working in an environment governed ...

Enter and maintain program, site, and patient-level data into the Clinical Trial Management System (CTMS). * Work with the supply chain team to coordinate and dispatch shipments of investigational ...

The Project Manager is responsible for managing a portfolio of clinical trials and research ... The projects encompass a variety of indications and trial phases and will include those in start-up ...

Minimum 10 years of clinical trial management experience in a biotechnology, pharmaceutical company ... or CRO. Biotechnology experience desirable. * Experience building and managing a high-performing ...

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 ...

Responsible for supervising the trial site and delegating all tasks associated with it * Oversee ... Great management and leadership skills * Fast paced and dynamic individual This company will ...

... Trial obligations, reporting to the Director of Clinical QA. You will work closely with Clinical ... Time management skills * Demonstrated strong work-ethic * Outstanding customer service approach

Are you a QA Manager that has experience Performing QA Duties to ensure manufacturing, testing and clinical trial activities that comply with GMP, GCP and other regulatory guidelines * Document ...

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 ...

Generate, analyse and interpret clinical trial data. * Develop and manage relationships with external KOLs. * Provide internal coaching and leadership to the medical affairs team. Your Background

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 ...