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Latest jobs in Pharma

MSI Pharma recruit for contract and permanent roles in Pharma, Medical Device and Biopharma companies across the globe.

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Medical Device

Auditors - Medical Device Clinical Research - Medical Device Materiovigilance - Medical Device Medical Communications - Medical Device Pharmacovigilance - Medical Device Quality Assurance & Validation - Medical Device Regulatory Affairs - Medical Device Research & Development - Medical Device Technical Operations - Medical Device Technical Specialists - Medical Device Technical Writers - Medical Device
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Global Clinical Supply Chain Manager

Negotiable | California

We are currently hiring a Global Clinical Supply Chain Manager for one of our Pharmaceutical clients based in Carlifornia, USA. This position is open to 100% remote (PST preferred). Primary responsibilities:* Manage drug supply activities related to planning, label development, label & pack, and distribution for one or more clinical programs.* Actively develops and oversees supply plans to ensure accurate and continuous supply to patients wh...

Clinical Trial Leader

Negotiable | United States of America

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 environment by inspiring and influencing and encouraging mutual respect, instills innovation and accountability on ...

Director - Drug Safety Physician

Competitive | England

MSI Pharma are working with a small biopharma company to help source a Senior Director Level Safety Physician. The client are looking for someone with at least 10 years' global safety experience, a strong academic record and clinical medicine experience in an advance medical setting. Required Qualification and Experience · Doctor of Medicine degree with at least 10-year experience in clinical and post-marketing safety and/or clinical development in the pharmaceutical or biot...

Consultant Drug Safety I


MSI are looking for Drug Safety Specialist to join a well known Biotech company based in the US. If you have any experience with ICSR's, case processing and working on a safety database and are looking for a change, then this role may be for you. Responsibilities: · Works with direct manager and other Global Patient Safety team members to execute submissions processes for generating, submitting, and tracking expedited individual case safety reports and aggregate safety repor...

Senior System Engineer

Negotiable | 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...

Veeva Vault

US$50 - US$65 per hour | California

System administration in Veeva Vault: Solution and/or maintain system workflows management of system access and permissions design solutions and manage configuration configure and manage integrations to Vault platform perform change management activities in support of vendor enhancements and customer requirements participate in the development of solutions and manage project/change timelines liaise with users to resolve issues oversee Veeva managed services resources define and o...

Patient Safety Physician Freelance

Negotiable | United States of America

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 working on Benefit and Risk analysis activities Experience working in a Pharma or Biotech company Main job activities:Con...

Pre-Clinical Study Manager

£40000 - £50000 per annum | Northamptonshire

MSI Pharma are seeking to fill a position for a Pre-Clinical Study Manager to manage a range of Non-Clinical studies for new product development based on global regulatory requirements. Key Responsibilities: Proficient in HPLC/TLC/LC-MS Analytical techniques. Experience in Project Management. Previous Experience in Study Director in a GLP facility. Exp...

Clinical Operations Manager - Remote - Biotech

US$130000 - US$150000 per annum

Clinical Operations Manager - Homebased in USA - Large Biotech - ASAP start dateSalary: 140,000 - 160,000 USD (depending on experience)Start Date: ASAP / March 2022Interviews from: 14th February 2022Accountable for the management, support and direct supervision to Clinical Operations staff across multiple therapeutic areas. Provides training, consultation and o...

Senior Clinical Research Associate

Competitive | 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 Abili...

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