Research Associate

Posted Yesterday
Be an Early Applicant
Berlin, DEU
In-Office
Entry level
Biotech
The Role
Performs and analyzes bioanalytical ligand-binding assays, including pharmacokinetic and anti-drug antibody studies. Maintains LIMS records, laboratory equipment, reagents, documentation, and sample information. Supports method development, validation, SOP compliance, data presentation, inventory management, waste handling, and laboratory safety practices.
Summary Generated by Built In

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

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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 [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

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

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The Company
HQ: Bethesda, MD
1,114 Employees

What We Do

Precision is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. This maximizes our clients’ insight into patient biology, delivering more predictable trial outcomes and accelerating clinical development. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.

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