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Clinical Operations Supervisor Iv

3-5 years
$105,000 – $140,000 annually
10 June 11, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Clinical Operations Supervisor – On-Site | Madison, WI

Job Summary:

Fortrea is hiring an experienced Clinical Operations Supervisor to lead clinical teams at its Phase I Research Unit in Madison, Wisconsin. In this fast-paced, on-site role, you'll directly manage cross-functional clinical teams conducting a wide variety of early-phase clinical trials, including first-in-human, food-effect, and drug-interaction studies. Ideal for candidates with clinical research leadership experience, this is an exciting opportunity to work at the forefront of drug development.


Key Responsibilities:

  • Supervise clinical staff (RNs, LPNs, CRCs, Technicians, etc.) in Phase I trials

  • Ensure compliance with ICH-GCP, SOPs, and study protocols

  • Lead staff training, scheduling, and performance evaluations

  • Manage clinical data quality, safety, and compliance documentation

  • Support protocol assignment, client visits, and quality initiatives

  • Coordinate staff development programs and continuous improvement projects

  • Ensure subject safety and ethical study conduct at all times

  • Create and maintain Standard Quality Procedures (SQPs) and Policies

  • Evaluate KPIs and optimize operational efficiency

  • Contribute to a culture of teamwork, safety, and excellence


Required Skills & Qualifications:

  • Bachelor’s degree in a science or medical field (or equivalent experience)

  • 5+ years of clinical research experience, with 3–4 years in a supervisory role

  • Strong understanding of ICH-GCP and regulatory compliance

  • Exceptional leadership, problem-solving, and communication skills

  • Experience in fast-paced, protocol-driven clinical trial environments

  • Preferred: Six Sigma Green Belt certification

  • Proficiency with electronic data capture (EDC) systems and clinical tech platforms


Perks & Benefits:

  • Comprehensive Medical, Dental & Vision Insurance

  • Life Insurance, Short/Long-Term Disability

  • 401(K) Retirement Plan

  • Paid Time Off (PTO)

  • Employee Recognition Awards

  • Multiple Employee Resource Groups (ERGs)

  • Career advancement in a global clinical research leader


Company Overview:

Fortrea is a leading global Contract Research Organization (CRO) operating in over 100 countries. With decades of experience across 20+ therapeutic areas, Fortrea partners with top pharmaceutical, biotech, and medical device companies to accelerate the development of innovative treatments. As part of our mission, we drive operational excellence through scientific rigor, global reach, and digital transformation in clinical research.


Work Mode:

On-Site – Madison, WI


Compensation:

Target Salary Range: $105,000 – $140,000 annually (based on title and experience)


Call to Action:

Ready to advance your leadership career in clinical research? Apply now to join Fortrea’s expert team in Madison, WI, and be part of the global mission to transform healthcare through cutting-edge drug development.