Our client, a world class pharmaceutical company driven by research and development, strives towards better health for individuals by developing safe, effective and innovative pharmaceutical products and now ranks as the fastest-growing among the UK''s top 50 pharmaceutical companies. They are seeking a GCP Compliance Specialist for their location in London.
JOB ROLE:The GCP Compliance Specialist will ensure that studies are conducted in accordance with applicable regulations and guidance
Support the clinical operations team
Quality management aspects for programs and studies
Investigator meeting attendance GCP quality system
Planning and oversight of audit activity and outcomes, including follow up and closure
Training and oversight of sub-contracted auditors
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:Life Science Degree
Solid experience in the Pharma industry or CRO
Expert knowledge of Clinical Trials, GCP regulations, EU and FDA
GCP Auditing experience including investigator sites
PERSONAL SKILLS & ATTRIBUTES:
Excellent communication skills both verbal and written
Organisation and planning skills
BENEFITS OF THE ROLE: This is one of the fastest growing pharmaceutical companies in the industry known for a culture that supports a unique work environment and encourages employees to focus on collaboration and personal development. The company values its staff and provides the framework to bring out the best in everyone, viewing investment in them as key to their success. You can earn an excellent remuneration for this role and enjoy all the benefits of a central London lifestyle.
Fforde is acting as a recruitment agency/business.
KEYWORDS: GCP Compliance Specialist, QA, Quality Assurance, Clinical Research, Clinical Study, Clinical Trial, Life Science, Degree, CRO, Pharmaceutical, Auditor, London, UK