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Senior Manager, Bioanalytical Services

6+ years
Not Disclosed
10 July 21, 2025
Job Description
Job Type: Full Time Education: PhD in Chemistry, Biochemistry, or related scientific discipline Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Summary:

ICON plc, a global leader in clinical research and healthcare intelligence, is hiring a Senior Manager, Bioanalytical Services for its on-site bioanalytical lab in Lenexa, Kansas. This full-time leadership position focuses on overseeing regulated LC-MS/MS operations, including method development, validation, and sample analysis. The role is ideal for experienced scientific leaders passionate about regulated bioanalytical workflows and high-quality drug development in a GLP-compliant environment.


Key Responsibilities:

  • Lead day-to-day operations of LC-MS/MS lab supporting regulated clinical studies.

  • Oversee development, validation, and execution of methods for small molecules, peptides, siRNAs, and ADCs.

  • Ensure all studies comply with GLP, ICH M10, and global regulatory guidelines.

  • Act as scientific liaison with clients, contributing to study design and issue resolution.

  • Collaborate with Business Development to support client acquisition and retention.

  • Represent LC-MS/MS operations in audits, regulatory inspections, and client meetings.

  • Manage lab resources, team productivity, and instrumentation capacity.

  • Mentor, coach, and develop a team of analysts and scientists.

  • Drive innovation, data integrity, and continuous process improvement.

  • Work cross-functionally with LIMS teams and other global bioanalytical sites.


Required Skills & Qualifications:

  • PhD in Chemistry, Biochemistry, or related scientific discipline.

  • Minimum 6 years’ experience in regulated LC-MS/MS bioanalysis.

  • Supervisory or leadership experience in a bioanalytical lab setting.

  • Expertise in chromatographic techniques and bioanalytical regulatory compliance.

  • Familiarity with automation tools, LIMS, and ELNs preferred.

  • Experience supporting audits and client communications.

  • Excellent communication, problem-solving, and mentoring capabilities.


Perks & Benefits:

  • Competitive full-time salary package (salary not specified; compensation is benchmarked to market).

  • Annual performance-based bonus.

  • Comprehensive health insurance for employee and dependents.

  • Retirement plans with employer contributions.

  • Life assurance and wellness programs.

  • Global Employee Assistance Program with 24/7 access to mental health professionals.

  • Flexible, country-specific optional benefits such as travel passes, gym discounts, and more.


Company Description:

ICON plc is a top-tier Clinical Research Organization (CRO) delivering high-quality drug development services across pharmaceuticals, biotech, and medical device sectors. With a strong focus on scientific innovation, regulatory compliance, and operational excellence, ICON enables faster and safer clinical trials across the globe.


Work Mode:

On-site – Lenexa, Kansas, USA
Employment Type: Full-Time


Call-to-Action:

Are you ready to lead cutting-edge bioanalytical operations in a GLP-compliant environment? Apply today to become part of a world-class scientific team at ICON plc and help drive innovation in global drug development.