- QA Specialist, Documentation
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life. ...
- Trial Documentation Specialist
The Trial Documentation Specialist will be involved in a variety of tasks, being responsible for maintaining Trial Master Files and performing quality checks within the given timelines. For this challenging role you should be highly detail-oriented with the ability to handle and prioritize multiple tasks, should be quality conscious and work as an effective team member thus contributing to the team’s growth.
- Principal Scientist - Separation Science
ProClinical is looking to recruit a Principal Scientist on behalf of our client, a global, well established vaccine company.Job Role: This Principle Scientist job will take a leading role in establishing strategy, development and validation of molecular biology and immunoassays for testing vaccine products. The candidate will be expected to work efficiently with cross-functional teams. ...
- Principal Clinical Data Manager - Antwerp
Laura Christie is recruiting for a Principal Clinical Data Manager for a CRO based in Belgium on a permanent basis.
Main duties and responsibilities
- Project Specialist
Freelance or Permanent Project Specialist (Serbia) required for an international company. If you are a Life Sciences Graduate, Nurse or a Pharmacist and are looking for a new contract this is the perfect match for you. ...
- Principal Scientist
Principal Scientist wanted for our Basel based client in the pharmaceutical sector.Your experience/skills: * Ph.D. ...
- Senior / Principal SAS Programmer - London
Opportunity to work for a specialist Biometric CRO who are looking for experienced Senior and Principal level Statistical Programmers to join their expanding Biometric team in London.
- Principal Statistical Programmer
Principal Statistical Programmer will serve as a Lead Programmer for projects and serve as contact with clients for programming aspects of clinical studies.
- Principal Clinical Data Manager
ProClinical is working with one of the top 10 pharmaceutical companies to find a Principal Clinical Data Manager that will focus on early-phase (Phase I & IIa) clinical pharmacology, patient, and Proof Concept / Proof Mechanism studies. This is a permanent role based in Uxbridge, UK. Job Role:This Principal Clinical Data Manager role is accountable for the execution of the Data Management (DM) Strategy of clinical drug programs (assets) in accordance with the Clinical Development Plan. ...
- Regulatory Documentation Scientist
Regulatory Documentation ScientistLeading Pharmaceutical company6 month contractFreelance opportunityFull time office based Hertfordshire (home working maybe possible for 2 days a week after the induction period)