Investigator Jobs in Wakefield
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Search results - Investigator Jobs in Wakefield
RBW Consulting-Wakefield
accountabilities
• Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites...
Meet Life Sciences-Wakefield
include (but are not limited to):
• Clinical study protocols
• Clinical study reports (CSRs)
• Executive summaries
• Common Technical Document (CTD) clinical summaries
• Investigator brochures (IBs)
• Clinical trial authorisation (CTA) documents
• Patient...
RBW Consulting-Wakefield
accountabilities
• Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites...
The Mullings Group-Wakefield
of the study EDC software, the electronic Investigator Site File (eISF), and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits to ensure CIP adherence and data integrity.
• Collaborate with investigators...
Hlx Life Sciences-Wakefield
investigational product inventory, reconciliation and storage at trial sites, ensure GCP guidelines are followed
• Reviews the Investigator Site File for accuracy and completeness
• Provides site and regional metrics into trackers to support project-level report...
Meet Life Sciences-Wakefield
as a lead author on multiple regulatory documents, including at least 3 of the following: protocols, clinical study reports, clinical summaries, clinical overviews, investigator brochures, narratives, briefing documents, or regulatory response documents...
Aurora Lifesciences-Wakefield
will manage and lead non-conformance investigations and document containment, root cause investigations. Furthermore you will provide technical leadership for a range of quality engineering activities including process change control, non-conformance...
Wakefield
regular stock checks to ensure accuracy and minimize discrepancies
Investigate stock-related issues and implement solutions promptly
Coordinate with warehouse and logistics teams to ensure efficient stock flow
Prepare reports on inventory status, movement...
cv-library.co.uk -
Aurora Lifesciences-Wakefield
investigations and document containment, root cause investigations. Furthermore you will provide technical leadership for a range of quality engineering activities including process change control, non-conformance investigations, SCARs, CAPA, quality continuous...
Peel Recruit-England
We are currently recruiting for a Mentor to Financial Investigators. Location: Multiple locations available (London, Sheffield, Cardiff, Manchester and Hounslow) Hours: Full time on site – 37 hrs per week Contract duration: Temporary ongoing...
mindmatch.ai -
Blush & Bloom Talent Ltd-Wakefield
performance and suggest improvements.
• Support root-cause investigations and recommend corrective actions for non-conformances.
• Evaluate new or alternative raw materials and test substitutions where needed.
• Ensure accurate and up-to-date technical...
Wakefield
and analyse data to determine required stock levels
• Raise purchase orders for stock
• Investigate and resolve warehouse queries relating to stock/batch discrepancies
• Raise stock transfers between locations
• Maintain...
cv-library.co.uk -
Planet Pharma-Wakefield
with the preparation of submission and other complex clinical documents.
As part of this role, you will be responsible for authoring most study-level documents including protocols, ICFs, lay summaries of clinical trial results, briefing packages, and investigator...
Warman O'Brien-Wakefield
at client and investigator meetings
• Preparation of biostatistics input to company research proposals and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client.
Key Qualifications and Skills
• M.S...
Planet Pharma-Wakefield
with the preparation of submission and other complex clinical documents.
As Senior Medical Writer, you will be responsible for authoring high complexity study-level documents including protocols, ICFs, investigator brochures and meeting packages. You will also...
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