Research Associate

Pfm · Berlin, Berlin, Germany · Other

Posted 2026-11-03

Apply for this role →

12 month Fixed Contract Role.

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

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

Essential functions of the job include but not limited to:

Completed degree in Biology, Biochemistry, Biotechnology, Pharmacy, Chemistry, or a comparable scientific discipline.

Initial experience in bioanalytics or ligand-binding assays (LBA) is an advantage.

Knowledge of PK (Pharmacokinetic), ADA (Anti-Drug Antibody), TAb (Total Antibody), and/or NAb (Neutralizing Antibody) analyses is desirable.

Experience working with LIMS systems, Microsoft Excel, and GraphPad Prism.

Careful, structured, and quality-oriented way of working.

Strong teamwork and communication skills.

Very good German language skills and good English language skills, both written and spoken.

Apply for this role →

← Back to all jobs