Regulatory Affairs Specialist
SciPro continues our long-standing exclusive partnership with a ground-breaking, medical device company who are the...
SciPro continues our long-standing exclusive partnership with a ground-breaking, medical device company who are the...
SciPro continues our long-standing exclusive partnership with a ground-breaking, medical device company who are the...
One of our valued pharmaceutical clients is looking for a QA professional to join their Quality Department in Cambridge on a full time on-site basis. This organisation has been researching, developing and supplying novel, effective and po...
One of our valued Rare Disease Pharmaceutical clients looking for a GCP Drug Development Quality Manager to join the clinical operations team and ensure the smooth running of development projects and QA strategy across multiple functions. ...
SciPro are currently working with a highly specialised, rare disease pharmaceutical company who...
SciPro are partnering with a growing independent pharmaceutical company who are seeking a Clinical Programmer...
Clinical Site Manager, UK Join a Clinical Operations team supporting the delivery of CRO services for global clinical trials. In this role, you’ll manage clinical study sites from qualification through to ongoing support, helping ensure i...
SciPro are partnering with a growing independent pharmaceutical company who are seeking a Clinical Programmer...