Planet Pharma is seeking an experienced Research Associate to join our client and work within the Bioanalytical and Molecular Assays team. This role plays a part in the advancing cutting edge science, that will support the growing mRNA pipeline and generate high-quality bioanalytical data that supports the development of innovative mRNA medicines and make a meaningful impact for patients worldwide.
This is a 6-month fixed-term contract opportunity.
Key Responsibilities
- Execute ligand binding and cell-based assay development and validation experiments following established protocols and study plans.
- Perform sample analysis for clinical specimens in accordance with approved procedures and regulatory requirements.
- Support assay development, validation and sample analysis activities to meet project timelines.
- Analyse experimental data using established methods and communicate results effectively to project teams.
- Perform critical reagent preparation and characterisation according to established procedures.
- Maintain accurate and complete experimental documentation using electronic laboratory notebooks.
- Assist with the preparation and maintenance of Standard Operating Procedures (SOPs), technical reports and scientific data presentations.
- Execute laboratory procedures in compliance with applicable GLP, GCLP, GMP and Client’s internal quality standards.
- Participate in routine laboratory maintenance, inventory management and equipment upkeep.
- Identify deviations or technical issues, communicate findings promptly and escalate concerns to senior scientists or management as appropriate.
- Collaborate effectively with colleagues to support departmental objectives and continuous improvement initiatives.
- Contribute to high-quality experimental execution and timely generation of bioanalytical data supporting assay development, validation and regulated clinical sample testing.
- Here’s What You’ll Bring to the Table:
Required Qualifications & Experience
- Bachelor’s degree in Biological Sciences or a related scientific discipline.
- Minimum of three years’ experience within a biotechnology, pharmaceutical or Contract Research Organisation (CRO) environment.
- Working knowledge of ligand binding assays and/or cell-based assays.
- Experience supporting pharmacokinetic (PK), anti-drug antibody (ADA) and/or neutralising antibody (nAb) assays is preferred.
- Experience working within a regulated laboratory environment operating under GLP, GCLP and/or GMP is preferred.
- Strong attention to detail with the ability to accurately follow established laboratory procedures.
- Excellent organisational, communication and time management skills.
- Demonstrated ability to manage multiple priorities while working collaboratively within a team environment.
- Commitment to producing high-quality work while maintaining compliance with laboratory quality systems.
This is a site-based position requiring full-time presence at Client’s Harwell site and is not eligible for remote working.
…
