ICON plc

Supervisor, Bioanalytical Services

ICON plc$88K — $105K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in relevant scientific discipline; advanced degree preferred.
  • 7+ years of experience with ligand binding and cell-based assays.
  • In-depth knowledge of bioanalytical laboratory operations and regulatory requirements.
  • Proven leadership experience in managing laboratory teams.
  • Strong analytical and problem-solving capabilities with attention to detail.
  • Effective communication skills for stakeholder engagement.

Responsibilities

  • Oversee daily operations of the bioanalytical laboratory for clinical projects.
  • Validate and perform assays on biological samples from clinical trials.
  • Review and sign off on data and quality control for various assays.
  • Manage compliance with regulatory requirements and standard operating procedures.
  • Plan and execute bioanalytical studies for pharmacokinetics and biomarkers.
  • Collaborate with project management and quality assurance teams for timely results.
  • Train and mentor laboratory staff to promote professional growth.

Benefits

  • Comprehensive health and wellbeing programs including medical, dental, and vision coverage.
  • Retirement and pension plans included.
  • Life assurance and disability coverage offered.
  • Access to employee assistance programs and wellbeing resources.
  • Structured training and career development opportunities.
Full Job Description
Supervisor, Bioanalytical Services-Ligand Binding Assays (LBA) - Clinical Research (CRO) - Lenexa, Kansas (KS)

We are seeking a full-time Supervisor, Bioanalytical Services for our Ligand Binding Assay team in the Greater Kansas City area!

As a Supervisor, Bioanalytical Services at ICON, you will oversee the daily operations of the bioanalytical laboratory, ensuring the accurate and timely analysis of biological samples to support groundbreaking clinical research projects. Your leadership will be vital in maintaining high-quality standards, optimizing laboratory workflows, and fostering a collaborative environment among team members.

What You Will Be Doing:

  • Responsible for assisting in the day-to-day activities of the bioanalytical laboratory including direct responsibility for validating and performing assays on biological samples from pre-clinical and clinical trials as needed.
  • Review and sign off on data and QC review of ligand binding assays including ELISA, ECLIA (MSD), ELLA, PK, ADA, NAb (neutralizing antibody), and other plate-based assays
  • Supervising and managing the bioanalytical services team, ensuring compliance with regulatory requirements and adherence to standard operating procedures (SOPs).
  • Overseeing the planning and execution of bioanalytical studies, including validation and sample analysis for pharmacokinetics and biomarkers.
  • Collaborating with cross-functional teams, including project management and quality assurance, to ensure timely delivery of accurate analytical results.
  • Implementing and monitoring quality control measures to maintain laboratory standards and continuous improvement initiatives.
  • Providing training and mentorship to laboratory staff, promoting professional development and a culture of scientific excellence.
  • Sets goals, assigns and coordinates tasks, ranks priorities, monitors performance, and evaluates performance.
  • Participate in conference calls with Sponsors on scientific matters.

Your Profile:

  • Bachelor’s degree in a relevant scientific discipline such as biochemistry, chemistry, or a related field; advanced degree is a plus.
  • 7+ years of experience with ligand binding and cell-based assays including but not limited to ELISA, ELLA, other plate-based assays
  • Significant experience in bioanalytical laboratory operations, with a strong understanding of regulatory requirements in the pharmaceutical industry.
  • Strong leadership skills, with experience managing teams and driving collaboration in a fast-paced laboratory environment.
  • Excellent analytical and problem-solving skills, with a focus on attention to detail and data integrity.
  • Effective communication skills, with the ability to build relationships and influence stakeholders at all levels of the organization.

#LI-KM3


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our to read more about the benefits ICON offers.

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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