PV Partner Management Associate
US$40 - US$47 per hour + negotiable
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United States of America
MSI Pharma are working with a leading Pharmaceutical company in the US who are looking for a Associate PV Partner Management Contractor to join their team on an ongoing long term project details below.Responsibilities:Process and Compliance:
Act as the process owner for business systems and contract repository for PV-related contracts.
Conduct planning activities related to system outputs as needed.
Develop and optimi...
Quality Learning Solution Specialist
Negotiable
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Denmark
Are you a passionate expert in Training and Learning Management for GxP regulated environments? Are clients as a leading IT solution provider seeking individuals like you to join their Quality Solutions Europe Team. In this role, you'll play a pivotal part in transforming traditional methods into smart, innovative solutions integrated into GxP frameworks. Location:Fully remote from most European countries. Responsibilities:- Dr...
Digital Operations Manager
Negotiable could also be part time
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Brussels
Established Biotech in Belgium need an experienced Digital Operations Manager to join their team on Freelance / contract (hourly rate basis). The initial assignment will be until February 2025. As a crucial link between their business and IT departments, you'll spearhead digital solutions for Neurology, Immunology, and Rare Diseases. With a focus on project management and marketing automations, you'll ensure seamless alignment between stakeholders and IT. This role involves rolling out...
Clinical Operations Intern
US$20 - US$25 per hour
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United States of America
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 to working with Clinical Operations study support, start start-up, study management, site management, and compliance...
Therapeutic Area Strategy Lead
Competitive
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United States of America
MSI are working with a well known Global Pharmaceutical company to source an experienced Safety Physician to join their team as a Therapeutic Area Strategy Lead. The main responsibilities of this role are:- Deputize for the TA Head: - In times of absence or unavailability - Matrix Leadership of Global Safety Officers (GSO) - Maintain Therapeutic Area expertise, product portfolio-specific expertise and ongoing assessment of therapeutic areas, competitive drugs an...
Automation Engineer
Negotiable
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Liverpool
Professional Automation Engineer role within the Liverpool site Automation Team responsible for the delivery of multiple PCS7/HMI/PLC upgrade projects. The role will involve execution of approved projects and development of new project proposals as part of the site's long term sitewide strategy to address control systems obsolescence. ResponsibilitiesResearches, evaluates and assesses installed PCS/HMI/PLC systems (Siemens, Mitsubishi,...
Senior System Engineer
Negotiable
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Switzerland
MSI are looking for Senior Process Engineers to join a Top Pharmaceutical Organisation based in the Switzerland. If you have any experience with DSP manufacturing and GMP within a Biotech of Pharma company and are looking for a change, then this role may be for you. Key Responsibilities:* Being domain expert for new and existing system related to DSP (Downstream Process) manufacturing of biotech products in the si...
Associate Director - Clinical Research
Competitive
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New Jersey
MSI are working with a a global leader in OTC products, who are seeking an experienced Clinical professional to join their team.The Associate Director - Clinical Research is a pivotal role and will work within a cross-functional global team and will require collaboration with a number of internal teams including Category and Regional Medical Affairs, Clinical Operations, Pre-clinical, Regulatory, Innovation, Statistics & Data Management as well as external groups, Clinical Research...
Regulatory Affairs Manager
Negotiable
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England
MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a UK based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the UK Responsibilites:Manage the timely preparation (may include authoring) and delivery of CMC contributions to the regulatory submissions linked to medicinal products throughout the lifecycle; including clinical programs mark...
Principle Medical Writer
Negotiable
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England
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 documents for more than 3 drug products in Oncology and Immuno-oncology
Leading the delivery for individual documents, setting clear expec...
