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MSI Pharma covers jobs in Pharma, Medical Device and Biopharma.
MSI have a wide variety of jobs in leading Pharmaceutical companies around the world
If you are looking for a permanent or temporary role in a Medical Device company, MSI can help
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€65 - €85 per hour | England
Large Pharmaceutical client in Belgium are looking for a dedicated IT Project manager with at least 5 years relevant experience who can start ASAP. The initial contract is 3 months but likely to extend into 2021 The role involves: - Coordination of small to medium projects in a GxP environment for the QA department - Act as analyst on QA-projects - Authoring and maintaining IT System documentation (such as Technical: user requirement specifications,...
Freelance CRA - Brazil - 1.0 FTE
€30 - €60 per hour + COMEPTITIVE | Brazil
Freelance CRA - Latin America countries - 1.0 FTE - Immediate start Freelance CRAs - various locations across Latin America There are multiple roles t - Site selection and site initiation visits- Feasibility/patient recruitment- Perform site inspections independently- Monitor patient safety on-site- Monitor and maintain ICH-GCP compliance- Perform close out visits- Assures compliance with local regul...
Change Management consultant
€90 - €105 per hour + part time or 5 days per week | England
My client is looking for several Change management consultants (Business transformation) for their global projects across all business sectors.Although infrastructure, technology skills are very important, the client have a stronger focus on the people and changing the way they work, whilst leading digital transformation.Major accountabilities: Diagnose: Assess change management needs (barriers/enablers) at different levels of the organization ...
Safety Scientist - Freelance
Negotiable | Basel
Global Senior Safety Scientist MSI Pharma is currently working with a Small Global Pharmaceutical company to help them hire a Freelance Senior Safety Scientist to join their team in Basel. Main Focus: · Manage case processing for clinical trials and electronic reporting to EMA; · Ensures oversight of our PV vendor · Manages interactions with internal departments as well as vendors, commercial partners and CROs · Coordinates and contributes to Develop...
Freelance Regulatory Affairs Consultant - IVD Expert
Up to US$999 per hour + COMEPTITIVE | New York
Freelance Regulatory Affairs Consultant - IVD Expert | Remote based (EMEA, APAC or US) To work for a Medical Device consultancy, responsible for global operations. We are looking for a someone to provide Regulatory Affairs consulting services within the IVD space. What will you be responsible for? - Regulatory consulting - IVDR transition and implementation - Pre-submission and clinical strategy support<...
Freelance Regulatory Affairs Consultant - IVD Expert - Remote
Up to £60 per hour + COMEPTITIVE | England
Freelance Regulatory Affairs Consultant - IVD Expert | Remote based (EMEA, APAC or US)To work for a Medical Device consultancy, responsible for global operations. We are looking for a someone to provide Regulatory Affairs consulting services within the IVD space.What will you be responsible for?- Regulatory consultancy - IVDR transition and implementation - Pre-submission and clinical strategy support-...
Clinical QA Director
US$165000 - US$205000 per annum | California
Overview: The Director, CQA will be a critical team member who designs and implements risk-based Clinical Practice (GCP), Good Laboratory Practice (GLP) Good Clinical Laboratory Practice (GCLP) and Good Pharmacovigilance Practice (GVP) audit programs and compliance oversight. This person will be responsible for activities that include assessing the effectiveness of GC, GLP, GCLP, and GVP processes, creating and presenting actionable reports, presenting data to Senior M...
Senior Drug Safety Scientist
Negotiable | Basel
Global Senior Safety ScientistMSI Pharma is currently working with Growing Biotech to help them hire a permanent Senior Safety Scientist to join their team in Basel. The team is currently small, so the new hire will have the chance to get involved with a wide range of safety activities with the end goal being a successful regulatory submission.Main Focus: To support the department head with scientific analyses, data reviews, signa...
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