Pharma jobs

• United States of America
• US$81 - US$86 per hour
• Posted 10 days ago

MSI Pharma are working with a leading Biopharma to help source a Global Quality Lead on a 6 month contract. As part of the Global Quality Assurance organisation, this position provides leadership and QA expertise in driving strategic and operational Quality Assurance activities. - Auditing experi...

• United States of America
• US$100 - US$115 per hour
• Posted 10 days ago

MSI Pharma are working with one of the top pharma companies in the world to hire a Quality Engineer for a 12 month contract. Tasks & Responsibilities: Supports the Product Release Monitoring and Strategic Collaborator Employee Certification Program. Reviews and approves key quality records as the...

• United States of America
• Negotiable
• Posted 11 days ago

My client is looking for several candidates with strong Veeva, RIMS experience for ongoing IDMP projects. Ideally you will have Veeva Vault Registrations - data model, business process, functional knowledge, coupled with Veeva Vault Product setup. Additional experience with RIM data analysis, dat...

• United States of America
• Negotiable
• Posted 11 days ago

Specialist Technology consultancy are looking for several dedicated Solution / Enterprise architects to join their European teams, in anticipation of the latest IDMP Regulatory changes effecting all life science companies that sell pharmaceutical drug products into EEA. The roles will be working ...

• United States of America
• Negotiable
• Posted 11 days ago

Global professional services Consultancy require several Data Scientists and Data Engineers for a project to start in November / December. The team of consultants will help with the continual advancement of their AI core extraction and classification engine by leveraging Natural Language Processi...

• United States of America
• Negotiable
• Posted 11 days ago

Following the latest EU IDMP Implementation guidelines, my client is looking for dedicated consultants to provide expertise and lead the delivery of projects involving implementation and/or management of Regulatory Information management (IDMP projects). The roles will heavily involve you advisin...

• United States of America
• Negotiable
• Posted 11 days ago

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Gui...

• England
• Negotiable
• Posted 11 days ago

Specialist Technology consultancy are looking for several dedicated Solution / Enterprise architects to join their European teams, in anticipation of the latest IDMP Regulatory changes effecting all life science companies that sell pharmaceutical drug products into EEA. The roles will be working ...

• England
• Negotiable
• Posted 11 days ago

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Gui...

• England
• Negotiable
• Posted 11 days ago

Following the latest EU IDMP Implementation guidelines, my client is looking for dedicated consultants to provide expertise and lead the delivery of projects involving implementation and/or management of Regulatory Information management (IDMP projects). The roles will heavily involve you advisin...

• England
• Negotiable
• Posted 11 days ago

Global professional services Consultancy require several Data Scientists and Data Engineers for a project to start in November / December. The team of consultants will help with the continual advancement of their AI core extraction and classification engine by leveraging Natural Language Processi...

• England
• Negotiable
• Posted 11 days ago

My client is looking for several candidates with strong Veeva, RIMS experience for ongoing IDMP projects. Ideally you will have Veeva Vault Registrations - data model, business process, functional knowledge, coupled with Veeva Vault Product setup. Additional experience with RIM data analysis, dat...

• United States of America
• Negotiable
• Posted 11 days ago

MSI Pharma are working with a globally recognised pharma company to help source a Senior Director Level Safety Physician to support the Hem-Oncology portfolio. The client are looking for someone with at least 8 years' global safety experience, a strong academic record and clinical medicine experi...

• United States of America
• Negotiable
• Posted 11 days ago

MSI Pharma is working with a global biopharma to source a Safety Writing Scientist to support the Global Patient Safety Unit for an initial 6 month freelance contract. The role: As the Safety Scientist, you will be writing benefit-risk assessments, safety risk management strategies, safety signal...

• United States of America
• Negotiable
• Posted 11 days ago

MSI Pharma are currently working with a mid-sized Global Pharma based in New Jersey to hire a Director level Freelance Safety Physician with experience undertaking benefit and risk analysis activities. The ideal candidate will have: Medical degree 5+ years' experience in Drug Safety Experience wo...

• United States of America
• Negotiable
• Posted 11 days ago

MSI Pharma are working with an innovative clinical-stage bio-pharmaceutical with a strong leadership group to source a Senior Safety Scientist to report into the head of the safety organisation. The company currently have a fully outsourced model but are in the process of bringing in-house a numb...