Senior Bioanalytical Study Manager
- Recruiter
- Confidential
- Location
- Reading
- Salary
- Competitive
- Posted
- 21 Jul 2021
- Closes
- 18 Aug 2021
- Sectors
- Health, Nursing & Social Care
- Contract Type
- Contract
- Hours
- Full Time
Highly rewarding opportunity to join the Bioanalytical project team of global biopharmaceutical organisation.
As Study Manager, you will call upon your thorough knowledge of large molecule bioanalysis and excellent communication skills to successfully interact with key project representatives at strategic vendors to execute method transfer, validation and sample analysis of PK, ADA and Biomarker studies.
Responsibilities
• Oversee method development & validation for various programs at CROs
• Ensure bioanalytical project tasks are executed to good scientific quality & deadlines are met
• Collaborate effectively with key business stakeholders
• Ensure harmonization of testing & reporting processes
Skills & Experience
• Extensive experience supporting regulatory bioanalysis in a pharma / CRO environment
• Excellent knowledge of a variety of large molecule techniques such as immunoassays & ligand binding assays
• Knowledge of GxP regulatory standards
• Excellent communication skills
Apply to VRS to be considered for this career defining opportunity!
Please note: This role is offered on an initial 12 month contract with realistic potential to be extended.
Key words: Bioanalytical, Large Molecule, LMB, PK, ADA, Biomarker, Pharmacokinetics, Immunogenicity, Immunoassay, Ligand Binding Assay, LBA, Method, Development, Validation, Transfer, Analysis, GxP, Regulations, Berkshire, Reading, Oxford, Slough, VRS7177CR
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Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website
As Study Manager, you will call upon your thorough knowledge of large molecule bioanalysis and excellent communication skills to successfully interact with key project representatives at strategic vendors to execute method transfer, validation and sample analysis of PK, ADA and Biomarker studies.
Responsibilities
• Oversee method development & validation for various programs at CROs
• Ensure bioanalytical project tasks are executed to good scientific quality & deadlines are met
• Collaborate effectively with key business stakeholders
• Ensure harmonization of testing & reporting processes
Skills & Experience
• Extensive experience supporting regulatory bioanalysis in a pharma / CRO environment
• Excellent knowledge of a variety of large molecule techniques such as immunoassays & ligand binding assays
• Knowledge of GxP regulatory standards
• Excellent communication skills
Apply to VRS to be considered for this career defining opportunity!
Please note: This role is offered on an initial 12 month contract with realistic potential to be extended.
Key words: Bioanalytical, Large Molecule, LMB, PK, ADA, Biomarker, Pharmacokinetics, Immunogenicity, Immunoassay, Ligand Binding Assay, LBA, Method, Development, Validation, Transfer, Analysis, GxP, Regulations, Berkshire, Reading, Oxford, Slough, VRS7177CR
Follow VRS Recruitment on LinkedIn to view all our latest vacancies!
Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website