Pharma jobs

• London
• Negotiable
• Posted 1 day 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 7 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...

• London
• Negotiable
• Posted 7 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...

• Belgium
• €80.00 - €82.00 per hour
• Posted 9 days ago

Business Analyst for AI-Driven Clinical Development We are looking for a dynamic Business Analyst to join our Digital Technology AI team, focused on supporting clinical development stakeholders. Your role will involve working on AI and GenAI solutions, enhancing documentation for clinical trials ...

• Anderlecht
• Negotiable
• Posted 10 days ago

My client in Belgium require a Business Analyst to join their Digital Technology team, reporting to the DT Lead AI for Clinical Development. The team builds AI solutions to streamline clinical development, accelerating drug delivery to patients. Due to nature of the work and team collaboration th...

• Brussels
• €35 - €50 per hour + negotiable
• Posted 11 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...

• United States of America
• US$20 - US$25 per hour
• Posted 11 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...

• Slough
• Negotiable
• Posted 11 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 11 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
• Negotiable
• Posted 11 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 11 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...

• California
• Competitive
• Posted 11 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 21 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...

• American Canyon
• Negotiable
• Posted 21 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...

• England
• Negotiable
• Posted 21 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 21 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...

• United States of America
• Competitive
• Posted 21 days ago

We are seeking a Senior Safety Physician for one of our international biotech companies. They are looking for someone with demonstrated experience answering challenging questions from health authorities and someone with in-depth knowledge of scientific data.

• United States of America
• US$20 - US$25 per hour
• Posted 21 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...

• England
• £50 - £65 per hour
• Posted 21 days ago

As the Project Manager for IT Clinical Insights projects (External), you will we be responsible for project management activities in projects focusing on delivering advanced analytics and visualisation for teams in clinical domain. The role can be based Globally. Your main responsibilities As the...

• England
• Negotiable
• Posted 21 days ago

MSI Pharma have partnered with a leading pharmaceutical company seeking a Principle Medical Writer. Experience More than 3 years of study related and submission related clinical regulatory documents Experience of writing protocols, CSRs, IBs, Briefing Documents Experience of writing relevant docu...