Research Associate

Precision Medicine Group; Berlin; Vor Ort; EUR 42.000 - 65.000; Vollzeit

Zusammenfassung

Precision Medicine Group is seeking a skilled biologist to plan, design, perform, and validate bioanalytical experiments based on ligand binding assays such as PK and ADA. The role involves conducting analyses on biological samples using established methods and maintaining rigorous documentation in SOPs and GLP/GxP practices.

You will manage data in LIMS, Excel, and GraphPad Prism, support associated LIMS processes, and help prepare overviews for development progress.

Qualifikationen

• Experience with PK/ADA methods or related ligand-binding analyses.
• Familiarity with GLP/GxP documentation and SOPs.
• Ability to manage samples and data in a regulated lab.
• Proactive in learning and following required SOPs.

Aufgaben

• Plan, design, perform, establish, analyze and validate bioanalytical experiments based on LBA formats (PK, ADA, TAb, NAb).
• Conduct biological sample analyses according to established methods.
• Self-train and comply with requirement documents.
• Analyze results within LIMS and Excel/GraphPad Prism.

Kenntnisse

Bioanalytical methods

Ligand binding assays

LIMS data handling

Microsoft Excel

GraphPad Prism

Laboratory safety

Tools

LIMS software

GraphPad Prism

Microsoft Excel

Jobbeschreibung

• Plan, design, perform, establish, analyze and validate Bioanalytical experiments based on Ligand Binding Assay formats (e.g., Pharmacokinetics and anti-drug antibody studies (PK, ADA, Total Antibody (TAb), Neutralizing Antibody (NAb)) per guided instructions for development of such methods
• Conduct biological sample analyses per established and trained ligand binding methods
• Self-train and compliance with requirement documents
• Analysis of results within Precision Laboratory Information Management System (LIMS), Microsoft Excel and Graph Pad Prism application
• Support of Laboratory Information Management System (LIMS) associated processes
• Aggregation of results for overviews or development progress in presentations or other document formats
• Review of study and department associated documents (e.g., SOPs, Validation Protocols, Validation Reports, Note to File documents, LIMS experiment protocols or protocol templates, and forms)
• Maintain equipment, fulfill responsibilities for specific equipment
• Responsibility for autoclaving liquid and solid waste
• Maintain overview of reagents stored at different storage temperatures, maintain the inventory of materials and reagents associated with all projects, and ordering
• Edit lab associated Clinical Sample information within applicable systems
• Assist in, contribute to establishing and improving, and comply with all procedures and required SOP documentation for PK or ADA methods and department associated documents
• Comply, maintain and support lab- and environment safety practices

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail] .

Candidates must be legally authorized to work in the country of employment without employer sponsorship.