Jobs · Analyst · North Carolina

Research Associate II

Elevait Solutions · Philadelphia, NC · Yesterday
On-siteAnalystContract

Key Responsibilities

  • Process and document whole blood samples from clinical studies in compliance with GxP and GLP/GCLP guidelines.
  • Cook up closely with clinical teams and laboratory managers for sample receiving, testing, and biobanking.
  • Execute immunoassays and cell-based assays (such as ELISA and ELISPOT) under supervisory guidance.
  • Analyze and report assay data accurately; contribute to technical reports and presentation materials.
  • Support new clinical assay development, including optimization, qualification, and troubleshooting activities.
  • Maintain meticulous lab documentation and recordkeeping per good documentation practices.
  • Track reagent and supply inventory for assigned projects; advise on procurement needs.
  • Author or contribute to standard operating procedures (SOPs) for new assays and laboratory equipment.
  • Help maintain a compliant and organized GxP laboratory environment.

Qualifications

  • Bachelor's degree in Immunology, Molecular Biology, Biochemistry, or related field.
  • At least 2 years of experience in regulated laboratory settings, preferably in clinical sample processing and immunoassay techniques.
  • Experience with ELISA, ELISPOT, and other immunoassay techniques.
  • Knowledge of Laboratory Information Management Systems (LIMS).
  • Experience with flow cytometry is preferred but not required.
  • Strong analytical skills and attention to detail.
  • Ability to work independently and as part of a team.
  • Good communication and organizational skills.

Preferred Skills

  • Experience with advanced immunoassays.
  • Experience with LabVantage LIMS.

Benefits

  • Flexible scheduling to accommodate critical sample support.
  • Opportunities for career advancement and skill development.
  • A supportive and collaborative work culture.
  • Prioritization of people and community.

Pay

Competitive salary commensurate with experience.

Schedule

Full-time position with flexible hours to support clinical trials.

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