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Medical Science Liaison Job Description Location: Hemel Hempstead (This role is an office-based role) Working hours: Monday – Friday, 9 am – 5.30 pm; 1 hour for lunch. Total weekly hours: 37.5 hours The company offers Flexible Working Times: Start anytime between 8:30 – 10:00 and finish afte...
We are seeking a dynamic senior Study/Trial Manager (CSPM) to lead our clinical trials with precision and expertise initially for a period of 6 months (with a view to potentially transition to a ...
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 ...
Proclinical is seeking a dedicated Manager of Global Trial Optimisation. This role involves overseeing the clinical development strategy, clinical study concepts and protocols as well as operational ...
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 ...
The Senior Manager, Global Trial Optimization (GTO) will lead program or study level activities to inform the clinical development strategy, clinical study concepts, study protocols and operational ...
Manage remediation and reconciliation projects * Support audits and inspections * Support ... Clinical trial lifecycle * TMF Reference Model (or equivalent) * eTMF systems * TMF Health ...
Minimum of 3-5 years' experience in the pharmaceutical industry with at least 5 years' experience in Regulatory Affairs including extensive global clinical trial experience. * Experience of managing ...
In addition, they will have proficiency in industry-standard clinical database applications, such as Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS). Experience with ...
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 ...
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 ...
With a rich blend of expertise in Clinical Development, Clinical Trial Supply, and Early Access ... Lead and manage projects involving Real World Evidence (RWE), integrating these insights with ...
Responsibilities Clinical Trial Conduct and Management: · Assist in the preparation of clinical trial documentation (e.g., regulatory submissions, study protocol update, IMPD amendment, etc.) · ...
Thinking creatively to identify and trial new approaches/ways of working to drive efficiency and ... Strong stakeholder engagement and management experience as well political awareness * Strong and ...
... trial. It's a demanding role that puts the successful individual at the heart of our dynamic ... Manage the sales cycle from start to finish - identifying and qualifying prospects, setting up ...
... trial and awareness of the brand and range of products • Work with wholesalers, buying groups and industry experts to always have a full pipeline of opportunities • Create and maintain ...
Ensure trial balances and balance sheet reconciliations are accurate for Group entities * Work with Treasury Management team on daily and medium-term cash flow preparation * Maintain sufficient funds ...
Preparation of month end to trial balance stage Banking * Purchase ledger entries using Dext * Regular bank reconciliations * Foreign exchange supplier management * Cashflow management via ...
Business Development Manager (AI Products) opportunity with an expanding AI product house based in ... lab-test and trial scalable business solutions in a reliable and secure environment
... trial balance level - Producing profit and loss reports and completing balance sheet reconciliation - Calculating, preparing and producing quarterly VAT returns and summaries - Assisting senior ...
Plan and manage regulatory submissions for clinical trial and marketing applications in compliance with global filing plans and local regulatory requirements. * Regulatory Strategy Implementation
Project Manager (BAT) 27-35k Plus Benefits + WFH 2 Days a Week WILL ALSO CONSIDER FREELANCERS ON ... THE ROLE Imagine yourself involved in the delivery of thrilling experiences that drive brand trial ...
Audit and Accounts Manager Camden £60,000 to £65,000 Butler Rose, public practice is delighted to ... Compile Profit and Loss accounts, balance sheets of assets and liabilities and trial balance ...