Bioanalysis Project Manager
Manage multiple bioanalysis projects.
Contribute to the development of a successful team.
Well-respected, growing company with great progression and a good range of projects.
This is an opportunity to join a leading company in the provision of bioanalytical and logistics expertise in scientific project management, contracted specialist services oversight and consultancy solutions within the international life sciences sector. This role requires expertise within Pharmacokinetic Bioanalysis, Antibody expertise and biomarker analysis. This Bioanalysis Project Manager will provide expert resource in bioanalytical scientific oversight, budgetary and project management of outsourced pharmacokinetic bioanalysis. What you'll be doing:
Providing oversight and management of method establishment, in assay validation and sample data review. Also providing expertise and knowledge within the areas of quantitative bioanalytical techniques, including mass spectrometric chromatographic and ligand binding assays.
Contribute to client project meetings, reviewing bioanalytical elements required in key planning and operational documents as well as keeping clients informed on project timelines.
Manage and liaise with various client functional/stakeholder groups involved in sample analysis and data processing including client CRO facing sample managers, CRO project pharmacology experts, data acquisition function and sample repository representatives.
Resourcing, selecting, and engaging suitable CRO bioanalysis providers for client projects.
Reporting to clients using data servers and various reporting processes on bioanalytical data generated by CROs (having created these reports).
Update and maintain CRO activity and KPI performance monitoring and tracking documents and tools as required by clients.
What experience you will need to apply:
Master’s Degree equivalent in Chemistry, Biochemistry, Biological science or similar discipline as well as relevant industry experience.
Extensive knowledge and experience in application and practice of bioanalysis within regulatory environments (GLP and GCP).
Comprehensive knowledge in design and execution of clinical and pre-clinical studies, toxicokinetic and pharmacokinetic analysis as well as understanding of the research activities undertaken within a drug development organization.
Practical experience within the pharma or CRO industry of managing and developing bioanalytical methods, assay validation and study data generation in clinical and pre-clinical studies.
Knowledge of the latest regulatory standards required for GXP studies including international guidance’s published by regulatory agencies such as FDA, EMA.
Engaging, enthusiastic, self-motivated, confident, solution orientated, self-assured and a team player. Willing to interact with both large global and emergent SME start-up organizations.
What you’ll get in return for your experience: Working from home with travel to the Kent based office required irregularly. Flexible style working hours. Travel expenses paid. 25 days holiday (plus bank holidays). Competitive salary with Discretionary rewards and recognition scheme. What’s next? If you’re looking for an exciting and challenging Bioanalysis Project Manager position speak to Jazz Jones.