Interim/Contract jobs

• Europe
• Competitive Salary
• Posted 11 days ago

​Source Clinical IT SME (Fully Remote- work from anywhere in Europe) The team is responsible for managing and supporting various Veeva Vault systems used for clinical development and quality management at UCB.

• Europe
• Competitive Salary
• Posted 11 days ago

​We are seeking a Consulting Project Manager to lead client implementation projects for technology solutions in the life sciences sector. This is a strategic, client-facing role requiring strong project management expertise, experience in regulated environments, and the ability to drive successful outcomes across global teams.

• Belgium
• Competitive Salary
• Posted 11 days ago

​We are looking for a Procurement Project Manager to support a major construction project in Braine l’Alleud. You will manage procurement across various projects, focusing on construction, MEP, and process equipment. This global role requires close coordination with the procurement team and adherence to regulatory requirements.

• Anderlecht
• Competitive Salary
• Posted 11 days ago

Lead, Global Talent, Compensation & HRIS Tools (SuccessFactors Focus) ​Experience Required: 5-8 years of experience in HR processes, talent management, performance, and compensation cycles. Strong background in SuccessFactors with a focus on functional and business advisory aspects. Experience su...

• Belgium
• Competitive Salary
• Posted 11 days ago

​We are seeking an experienced Procurement Manager based in Belgium to provide support for Building & Facilities procurement activities, including a major CAPEX project in the UK. The role requires independent work, strong knowledge of construction/facilities procurement, and experience in contract negotiation and vendor management. Immediate availability is essential, with potential for extension.

• Belgium
• Competitive Salary
• Posted 11 days ago

​The IT Veeva Vault Quality Configuration Specialist will play a key role in managing, configuring, and improving the Veeva Vault Quality Suite (including Quality Docs and QMS) for a global pharmaceutical company. Based in Belgium with hybrid work flexibility. Ideal candidates will have experience in Veeva Vault, Quality Assurance, system administration, and Pharma IT compliance (CSV/GxP). Strong communication, adaptability, and technical skills are essential.

• Belgium
• Competitive Salary
• Posted 11 days ago

​Join our international team as a Device Quality Lead, supporting the development and quality management of innovative medical devices like auto-injectors and pen injectors. This remote-friendly role (with some EU travel) is ideal for candidates experienced in ISO standards, supplier management, and risk control. Fluency in English is required; French is a plus. Help shape safer, smarter healthcare solutions — apply now!

• Belgium
• Competitive Salary
• Posted 11 days ago

​UCB is hiring a Device Documentation Lead (remote, Belgium-based) to support regulatory documentation for a drug-device combination product. Perfect for detail-oriented professionals with a collaborative mindset.

• Belgium
• Competitive Salary
• Posted 11 days ago

​We're seeking a CSV Expert with strong PCS 7 experience to support the qualification, validation, and remediation of computerized systems for a major biopharma building expansion project in Belgium. The role requires 8+ years of CSV experience, deep GMP knowledge, and strong collaboration skills. Primarily on-site with up to 60% remote flexibility.

• Belgium
• Competitive Salary
• Posted 11 days ago

Lead the selection and assessment of drug delivery devices for global clinical trials. Requires 8+ years’ experience, strong knowledge of medical devices and regulations (EU MDR, ISO13485), and a background in clinical trials. Work remotely from Belgium with a global, cross-functional team.

• England
• £50 - £65 per hour
• Posted 24 days 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...

• Kankakee
• US$55 - US$95 per hour
• Posted 24 days ago

Key Responsibilities: - Learn manufacturing processes from various site perspectives, including Fractionation, Bulk Purification, and Fill/Finish as applicable. - Support deviations and batch release from a process engineering perspective. - Use worst-case data, downscale reports, etc., to draft ...

• Buckinghamshire
• Negotiable
• Posted 24 days ago

My client, a globally renowned leader in the Consumer healthcare industry, is dedicated to delivering innovative skin health solutions. They are currently seeking an experienced Senior Regulatory Affairs Executive to join their dynamic Regional team on an initial 6-month contract. This role offer...

• London
• Negotiable
• Posted 24 days ago

Are you ready to thrive in a remote, flexible work environment? We're looking for a Senior Labelling Strategist specialising in regulatory labelling to join our client's team, collaborating with top Pharmaceutical companies through a leading service provider. For UK candidates the role will be in...

• United States of America
• Negotiable
• Posted 24 days ago

Responsibilities: Create documents for all phases of drug development, including manuscripts, abstracts, posters, oral presentations, and slide sets through their lifecycle. Independently write first drafts from study reports and/or source data, including primary and secondary analyses, with inpu...

• Belgium
• €80.00 - €82.00 per hour
• Posted 24 days ago

Business Analyst for AI-Driven Clinical Development We are looking for a dynamic Business Analyst to join our Digital Technology AI team, focused on supporting clinical development stakeholders. Your role will involve working on AI and GenAI solutions, enhancing documentation for clinical trials ...

• United States of America
• Negotiable
• Posted 24 days 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...

• Slough
• Negotiable
• Posted 24 days 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...

• American Canyon
• Negotiable
• Posted 24 days 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
• US$20 - US$25 per hour
• Posted 24 days 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...