Pharma jobs

• England
• Negotiable
• Posted 5 days ago

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....

• France
• Competitive
• Posted 5 days ago

MSI are seeking to fill a position for a Medical Science Liaison for a well known global pharmaceutical company. Responsibilities Reporting to the MSL Manager, the Medical Science Liaison is responsible for the implementation of the local affiliates Medical Plan and tactics that support the succe...

• American Canyon
• Negotiable
• Posted 5 days ago

MSI Pharma are working with a globally recognised pharma company to help source a PV Operations Associate. The ideal candidate will provide operational support to the US Patient Safety Clinical and Vendor Oversight teams to ensure proper performance of baseline PV compliance-based responsibilitie...

• United States of America
• Negotiable
• Posted 5 days ago

Responsibilities: Create documents for all phases of drug development, including manuscripts, abstracts, posters, oral presentations, and slide sets through their lifecycle. Independently write first drafts from study reports and/or source data, including primary and secondary analyses, with inpu...

• California
• Competitive
• Posted 5 days ago

MSI Pharma are partnering with an exciting biopharma based in California to source an experienced PV Operations Manager, at an Associate Director level. The main responsibilities for this role is: Manage Vendor Oversight including tracking of KPIs, metrics and QC of SAE/ICSR cases in Safety datab...

• United States of America
• Negotiable
• Posted 5 days ago

MSI are looking for a Clinical Trial Leader to join a prestigious Biotechnology company based in the West Coast (USA) accountable for the strategic planning and execution of assigned early development global clinical trials. Responsibilities: Displays leadership by creating a positive work enviro...

• California
• Competitive
• Posted 5 days ago

MSI Pharma are working with a small bio pharmaceutical company to seek an experienced Safety Medical Director to join their Neurology team. The main responsibilities for this role is: * Performs individual case report assessment and determines regulatory reporting responsibilities as required * P...

• Slough
• Negotiable
• Posted 5 days ago

MSI Pharma are looking for a Clinical Project Manager to join a prestigious Biotechnology company based in the UK accountable for leading Clinical Study Teams across Phase 1 studies. Responsibilities: At the study kick-off meeting, articulate study scope, goals, and expectations of the business t...

• Township of American
• Negotiable
• Posted 5 days ago

Our client, a global pharmaceutical company, are seeking a highly motivated Data Scientist to join their Data Sciences group. The Data Sciences team is seeking a Senior data scientist with expertise in machine learning, multivariate analysis, data engineering to support the CMC activities in the ...

• United States of America
• US$20 - US$25 per hour
• Posted 5 days ago

MSI Pharma are seeking to fill a position for a Top Biotech Organisation based in the USA. The client is looking for Clinical Operations Intern with Data entry experience. General Duties: Support tasks related to clinical trial study start-up, maintenance, and close-out, including but not limited...

• City of Brussels
• €35 - €50 per hour + negotiable
• Posted 5 days ago

MSI Pharma are working with a leading pharmaceutical company in Belgium who are looking for a Learning Contractor Specialist to join their team. Job Summary: Seeking a detail-oriented Learning Coordinator Specialist to join our team. Responsible for managing day-to-day operations, training progra...

• London
• Negotiable
• Posted 5 days ago

Job Title: Senior Regulatory Systems & Strategy Manager Location: EU Remote (Greater London) Salary: Up to £85,000 + benefits A leading technical service provider is seeking a Senior Regulatory Systems & Strategy Manager to support compliance with evolving regulatory requirements. In this fully r...

• London
• Negotiable
• Posted 5 days ago

Are you ready to thrive in a remote, flexible work environment? We're looking for a Senior Labelling Strategist specialising in regulatory labelling to join our client's team, collaborating with top Pharmaceutical companies through a leading service provider. For UK candidates the role will be in...

• Buckinghamshire
• Negotiable
• Posted 5 days ago

Immediate Opportunity: Regulatory Affairs Specialist (Medical Devices) Our client in the Buckinghamshire/Berkshire area is urgently seeking a Regulatory Affairs Specialist (Medical Devices) for a full-time hybrid role. This position offers a dynamic work environment and the chance to make a signi...

• Buckinghamshire
• Negotiable
• Posted 5 days ago

My client, a globally renowned leader in the Consumer healthcare industry, is dedicated to delivering innovative skin health solutions. They are currently seeking an experienced Senior Regulatory Affairs Executive to join their dynamic Regional team on an initial 6-month contract. This role offer...

• City of London
• Negotiable
• Posted 5 days ago

Responsibilities: Lead/support the planning and execution of the logistics required for assigned training events and team or leadership offsites, including scheduling and coordinating calendars, communications, production and dissemination of training materials, ordering meals, tracking participa...

• London
• Negotiable
• Posted 5 days ago

My client is seeking an experienced Sales Executive with a solid background in Life Sciences. Recognised for delivering cutting-edge Data services, they are a fast-growing provider of complex IT solutions within Regulatory, Quality, and Safety. What You'll Do: Lead end-to-end sales for Data Migra...

• Newark
• US$55 - US$65 per hour
• Posted 5 days ago

- Provide technical writing support for operational functions, particularly Quality Control (QC). - Author laboratory investigations for Out of Specification (OOS) events, deviations, CAPA, and change controls. - Perform risk analysis to determine the severity and likelihood of recurrence during ...

• Hopewell
• £70 - £80 per hour
• Posted 5 days ago

Key Responsibilities: Oversee day-to-day management of GMP paperwork, including reviewing and approving logbooks, analytical raw data, environmental monitoring reports, and other documentation. Support QA activities within the Warehouse, production areas, QC laboratories, and facility/utility spa...

• Kankakee
• US$55 - US$95 per hour
• Posted 5 days ago

Key Responsibilities: - Learn manufacturing processes from various site perspectives, including Fractionation, Bulk Purification, and Fill/Finish as applicable. - Support deviations and batch release from a process engineering perspective. - Use worst-case data, downscale reports, etc., to draft ...