Interim/Contract jobs

• Slough
• Negotiable
• Posted about 23 hours 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...

• Brussels
• €35 - €50 per hour + negotiable
• Posted about 23 hours 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
• Negotiable
• Posted about 23 hours 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...

• England
• £50 - £65 per hour
• Posted about 23 hours 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...

• United States of America
• US$20 - US$25 per hour
• Posted about 23 hours 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
• Negotiable
• Posted about 23 hours 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...

• American Canyon
• Negotiable
• Posted about 23 hours 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...

• United States of America
• Negotiable
• Posted about 23 hours ago

Job Responsibilities: Develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas. Develop and maintain an expert understanding of the safety profile of the assigned product(s) as well as understanding of the relevant strategic context (e.g., disease ...

• United States of America
• Competitive
• Posted about 23 hours 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.

• Braine-l'Alleud
• Negotiable
• Posted about 23 hours ago

MSI Pharma is partnering with a global biopharmaceutical company, and one of the world leaders in cutting-edge scientific research on a Cleaning Validation Engineer role. Start date: ASAP Duration: 3 Month Contract (Possibility of Extension) Location: Braine-l'Alleud, Belgium This is a collaborat...

• United States of America
• US$20 - US$25 per hour
• Posted about 23 hours 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...

• North Carolina
• Negotiable
• Posted about 23 hours ago

A global biotechnology organisation based in North Carolina is looking for a Quality Control Analyst to join the team on an initial 12-month contract. Responsibilities The primary responsibilities for this position include performing various tasks associated to QC support. Be responsible for ensu...

• United States of America
• Competitive
• Posted about 23 hours ago

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 mo...

• Visp
• €100 - €120 per hour
• Posted about 23 hours ago

MSI Pharma have partnered with a global partner to the pharmaceutical, biotech and nutrition markets. They focus on enabling treatments that prevent illness and support healthier lifestyles using scientific innovation and manufacturing technology to enable our customers to serve their patients an...

• England
• Negotiable
• Posted about 23 hours ago

MSI Pharma are seeking for a clinical project manager responsible for delivery of all aspects of global clinical studies. You will lead and maintain oversight for cross-functional teams comprised of internal and external partners. Ensuing delivery of clinical studies are done effectively and in a...

• London
• Negotiable
• Posted 5 days ago

Service Provider to the Pharmaceutical Industry Requires a Regulatory expert to Join their dynamic team as a Labeling Strategist, ensuring regulatory excellence in the pharmaceutical industry. Responsibilities and Experience: Hold a Bachelor's degree in a scientific discipline with 9 years' exper...

• Belgium
• €85.00 - €90.00 per hour
• Posted 9 days ago

Job Summary: (Have to be based in Belgium) We are seeking a highly skilled and experienced Senior IT Security Consultant, specializing in Vulnerability Management, to join our team at a leading pharmaceutical company. The ideal candidate will have a minimum of 5 years of experience in the field, ...

• Hopewell
• Up to US$50 per hour
• Posted 26 days ago

Job Title:QA Document Coordinator Duties: Assist with site documentation needs ensuring GMP compliance of day-to-day operations. Support Document Control Team with the formatting of procedural and technical documents, MBRs, and other GMP related documents. Process documents through the Veeva Qual...

• Braine-l'Alleud
• Negotiable
• Posted 26 days ago

Well-respected Biotech in Belgium need a VQL for an initial 12-month assignment to Join their dynamic team, driving strategic and operational Quality Assurance activities for Global Vendors in GMP manufacturing. You will Collaborate with internal stakeholders, manage deviations, KPIs, Quality Agr...

• Bern
• CHF hourly rate paid
• Posted 26 days ago

Our client in Switzerland, (Bern), require a dedicated CSV contractor to join their team in the New Year. The client prefer local candidates (Swiss permit holders) or EU citizens who can relocate to Switzerland within short notice. MSI are able to offer a competitive hourly rate for the position,...