Laboratory Digitalisation Partner (Data Integrity)
Negotiable
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Braine
As a Laboratory Digitalization Partner, you will be responsible for all aspects of digitalization and data integrity of the QC and In Process Control laboratories of the Manufacturing Engineering & HSE department, be it for the operational use of laboratory equipment, new equipment projects, electronic transformation projects of laboratory processes.You will join a dynamic and motivated team of four experts reporting to the Equipment and Data Integrity Manager, interacting with the...
Quality Control Analyst
Negotiable
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North Carolina
Quality Control Analyst - North Carolina US - Contract, Ongoing - Competitive Hourly Rates MSI have partnered with an exciting pharmaceutical company who are involved in the manufacturing of life-saving vaccines and medicines. They are looking for a Quality Control Analyst with knowledge of analytical methods and instrumentation. Some laboratory experience preferred. Key Responsibilities inclu...
Clinical Research Associate
Competitive
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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
Ability to manage required travel of up to 60% on a regular basis
Kn...
Data Governance - Veeva
Negotiable
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England
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 Guide EU IG v2.2 with the latest version due to be out soon, my client are looking for an experienced IDMP consultant to support the data Governance team and assess the impact on the implem...
Senior Pharmacovigilance project manager
£350 - £450 per day
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England
Senior Pharmacovigilance Project Manager - Contract Day-to-Day DutiesLeads small projects or supports large projects/programmes. Main focus will be support to oversight of outsourced services for patient safety, including those relating to the Covid-19 vaccine. The individual has a working knowledge of project management methodologies, tools and templates and contributes to the development and maintenance of work products or change pr...
Associate Director Cell Therapy Process Development
Negotiable
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United States of America
Associate Director Cell Therapy Process Development - Research & Development - East Coast The Genomic Medicine Unit (GMU) CMC group at the company is dedicated to the establishment of best-in-class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors, lentiviral vectors and cell therapy products.Our client is looking for an experienced cell culture development professional wi...
Medical Device - Regulatory Affairs Contractor
Negotiable
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Zuchwil
MSI Pharma is partnering with for one of the largest and diversified healthcare organizations in the world, on a MDR - RA role till 31/12/2023. This is a collaborative role supporting the local regulatory team for various activities in conjunction with MDR compliance work. This role will involve supporting the RA Business Lead in the development and creation of IT System documentation for new functionality related to Technical Documentation requirements, business improvements an...
Bioanalytical Scientist
Negotiable
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Kankakee
We are hiring a Bioanalytical Scientist Sr candidate for one of our pharmaceutical clients based in the US. Key responsibilities for this role include: * Develop and validate phase appropriate fit-for-purpose method for plasma proteins, impurities and excipients.* Utilizing AQbD approach to support In-Process, Finished Product Release and Enhance Characterization testing to support process development and clinical material production support.* This role will b...
PV Case Management Head
Competitive
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United States of America
MSI are working with a globally recognised pharma company to help source a PV Case Management Head. The client are looking for someone with significant global experience and a strong knowledge of the case management and medical safety evaluation in clinical trial and marketed products. Responsibilities for this role include: · To improve and reinforce globally integrated case management standards, procedures, and systems in line with changes in the regulatory environment and best ...
Safety (PV) Scientist - Freelance
Negotiable
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United States of America
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 assessments, regulatory submissions, aggregate reports, and publications.
You will lead the preparation of Patient Safety deliverables, including pla...
