Randox Clinical Laboratory Services [Genomics Services Group] require an experienced Clinical Scientist to work with the existing team developing new NGS tests and reporting genomic test results.
The main purpose of this post is to assist in development of new tests, production of automated reporting systems and to prepare clinical interpretative reports when required.
The person must be registered with HCPC [Health and Care Professions Council UK] as a Clinical Scientist.
You'll be joining a highly experienced team and helping to push their projects through clinical studies.
You'll be joining an innovative biotech company who are further expanding their team after a large funding round is expanding to support the Clinical Development of their pipeline as they move their lead asset into Phase 1 trials.
Hays have been exclusively retained by an extremely well-funded biotech driving breakthrough innovations in the space of gene therapy.They have developed an innovative new technology that allows them to deliver gene therapies in a novel way to patients with rare diseases and are currently going into their initial clinical trial to validate its use.
Alongside this they have multiple other programmes approaching the clinic and several more in development, giving them a very strong pipeline.The company prides itself on innovation and collaborative work and has a very experienced senior leadership & technical team coupled with a C-suite with a truly impressive track record.
This opportunity will provide a key support to the global team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program.
SRG are partnered with a leading Global Pharmaceutical Company who have an opportunity for a Clinical Scientific Expert to support the business on an initial 6 month contract.
This is a full-time role based primarily in Dublin, although some hybrid working is available.
Yolk Recruitment has a new opportunity for a Clinical Trials Manager to join an expanding manufacturer who are leading competitors within the Medical Sector.
Duties will include designing plus authoring trial documentation and regulatory submissions, plus monitoring the progress and performance of multiple trials from participant identification and recruitment through to ensuring reliable data collection.
This role reports directly to the Director of Clinical Affairs and is an opportunity for an established Clinical Trials Manager to join a secure company who offer professional growth and development.
We want all our employees to feel valued and engaged and are committed to offering a positive working culture along with a good work-life balance.
As well as ensuring they pay their employees fairly, they offer the following benefits: Flexible working, Generous annual leave, Pension Scheme, Sick Pay, Death in Service, Employee Assistance Programme, Bike Loan Scheme, Cycle2Work Scheme, Eyecare, Discount Portal, Social Activities.