Key duties will include:

• Act as Responsible Scientist or Principal Investigator (study manager) on assigned GLP and GCP studies
• Key point of contact for client (Sponsor) communication, building strong relationships
• Scientific review and approval of bioanalytical studies and related documents
• Generation of bioanalytical study plans and study reports
• Effective communication with mass spec analysts when instructing and organising laboratory work for coordination of analytical studies
• To ensure all work is performed efficiently to regulatory standards whilst meeting Sponsor deadlines
• Support the mentoring and training of more junior staff/analysts

The requirements:

• You will ideally be educated to degree level or a higher degree in a relevant scientific subject
• At least 5 years’ experience of work in a Bioanalytical GLP environment is essential.
• Experience acting as primary contact with Study Sponsors, preparing study plans and writing study reports
• Experience in analysis of a range of analytes including small and large molecule drugs and biomarkers
• Strong troubleshooting, data analysis and interpretation skills
• Proven organisational skills, self-motivated and attention to detail
• Able to communicate effectively
• Good planning and problem-solving ability
• A thorough approach to record keeping and documentation
• Good time management, decision making and prioritisation skills

The grading of this role is flexible dependant on experience and relevant qualifications.

If you are looking to advance your career, are seeking new challenges, opportunities and eager to expand your knowledge of regulatory quantitative bioanalysis and enjoy working in a dynamic and diverse team, then YBS is where you can make a difference.