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Clinical QA Compliance Specialist

€85.00 - €90.00 per hour | England

Summary: The Clinical Quality Assurance/Compliance Specialist will play a crucial role in ensuring compliance with regulations, guidelines, and study conduct within clinical trials. This individual will provide ongoing compliance support to studies, review study-specific documents and trainings, conduct compliance checks and inspections, manage risks and issues, and support audits, inspections, and deviation/CAPA processes. The ideal candidate will have 3 to 5 years of solid ...

Regulatory system advisory consultant

Negotiable | London

My client, a leading provider of IT solutions to the life sciences industry, is seeking to expand its Regulatory (System) advisory team and needs two experienced business consultants/managers.You will be tasked with leading the implementation of state-of-the-art business solutions for life science clients. This role is based in the UK, with the option for EU citizens to work fully remotely. To be considered, you must have previous experience in a life sciences (R&D) management cons...

Clinical system advisory consultants

Negotiable depending on experience | London

My client, a leading provider of IT solutions to the life sciences industry, is seeking to expand its Clinical operations advisory team and needs two experienced business consultants/managers.You will be tasked with leading the implementation of state-of-the-art business solutions for life science clients. This role is based in the UK, with the option for EU citizens to work fully remotely. To be considered, you must have previous experience in a life sciences (R&D) management cons...

Clinical Study Manager

Negotiable | United States of America

MSI Pharma are seeking to fill a position for a Top Biotech Organisation based in the West Coast. The client is looking for Clinical Study Managers who will lead all aspects of assigned clinical trials and demonstrate a high level of knowledge of clinical operations. General Duties: Works to ensure adherence to a standardized approach to clinical trial management Manages clinic...

Senior Clinical Research Associate

Competitive | United States of America

MSI is looking for Experienced Clinical Research Associates who are looking to grow with a Global CRO based in the USA. It is a homebased role with regional travel and the CRO is offering roles within exciting therapeutic areas! Education and Experience: Minimum 3+ year of Independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation Abili...

Pre-Clinical Study Manager

£40000 - £50000 per annum | Northamptonshire

MSI Pharma are seeking to fill a position for a Pre-Clinical Study Manager to manage a range of Non-Clinical studies for new product development based on global regulatory requirements. Key Responsibilities: Proficient in HPLC/TLC/LC-MS Analytical techniques. Experience in Project Management. Previous Experience in Study Director in a GLP facility. Exp...

Quality Assurance Specialist CSV

Negotiable | Switzerland

MSI Pharma are working together with a multinational manufacturing company in Switzerland seeking an experienced Quality Assurance specialist CSV. Key Responsibilities Responsible for Computerized System Validation (CSV) deliverables for new Large Scale Mammalian facilities, equipment and utilities related to the GMP manufacturing of biologics Representative of Quality in the CAPEX project organization in regards to CSV Reviewing and ...

Technical Project Manager - Industrial Automation & Integration

Negotiable | Switzerland

MSI Pharma is partnering with a global pharmaceutical leader on an exciting Technical Project Manager role on an initial 13 month contract....

Principal Pre-Clinical Research Scientist

Negotiable | England

MSI Pharma have partnered with a world-leading pharmaceutical company, they are currently looking an experienced Principal Pre-Clinical Research Scientist. You would be joining the Pre-Clinical Development team and be involved in innovating their global portfolio of leading consumer health drugs. Responsibilities Provide scientific and technical input to pre-clinical development plans Responsible for the design, implementation, and publication of pre-/ clinica...

Associate Director, Regulatory Affairs

US$150000 - US$180000 per annum + Bonus and Benefits | California

MSI Pharma is currently hiring a Regulatory Affairs Associate Director for one of our Pharma clients in the US. The Associate Director Regulatory Affairs will be responsible for the regulatory review and approval of all labeling, based on development and management of a target product profile (TPP);Oversee and coordinate the regulatory review and approval of all commercial materials through the Promotional Review Committee (PRC) and interactions with the FDA Offic...

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