Job Title:
Clinical Operations Supervisor II
Location: Dallas, TX (On-Site)
Category: Clinical
Job ID: 254595
Company Overview
Fortrea is a leading global contract research organization (CRO), operating in ~100 countries with a focus on scientific rigor and innovation. We partner with pharmaceutical, biotechnology, and medical device companies to transform drug and device development. Our culture—Fortrea FOUR—emphasizes:
Forward Together
Own It
Uphold Integrity
Respect People
Learn more at www.fortrea.com.
Position Summary
The Clinical Operations Supervisor II is a full-time, on-site role responsible for leading and supervising clinical staff (RNs, LPN/LVNs, Research Technicians) in a fast-paced Early Phase Clinical Research Unit. This role ensures the successful conduct of clinical studies in compliance with protocols, SOPs, ICH/GCP standards, and company quality expectations.
Key Responsibilities
Leadership & Supervision
Supervise and manage clinical operations staff (RNs, LVNs, Research Technicians).
Provide coaching, mentoring, and performance management.
Participate in hiring, training, disciplinary actions, and terminations.
Study & Protocol Management
Ensure studies are conducted per protocol, SOPs, and GCP standards.
Participate in planning study setup and investigator scheduling.
Assist with study procedures and protocol coordination when needed.
Training & Compliance
Ensure staff training programs are in place and up to date.
Maintain training documentation per SOPs and GCP.
Develop or update SOPs and Policies & Procedures (P&Ps) relevant to the role.
Quality Assurance
Maintain data quality and integrity.
Monitor and ensure safety and regulatory compliance.
Address and resolve GCP/ICH deficiencies.
Operational Excellence
Ensure staff levels meet forecasted workload.
Meet departmental KPIs and budget targets.
Contribute to continuous improvement and best practice implementation.
Maintain a safe, compliant, and high-quality work environment.
Required Qualifications
Education:
BS in Science or Medical field, OR
LPN/LVN or Associate Degree
Additional experience may be considered in lieu of formal education.
Experience:
Minimum 3–5 years of people management/direct reports experience.
Experience in clinical trials or a fast-paced clinical setting.
Certifications:
Six Sigma Green Belt preferred.
Skills & Competencies:
Strong understanding of ICH/GCP standards.
Excellent English (written and oral).
Effective leadership, time management, and problem-solving skills.
Able to adapt quickly to changing priorities.
Comfortable using technology in a clinical environment.
Work Conditions
Must be able to:
Stand/bend for up to 6 hours/day.
Use hands for computer work for up to 6 hours/day.
Distinguish colors and hear adequately for job functions.
Work Schedule: Overtime and weekends as required.
Must meet mandatory immunizations and screening requirements.
Handling of biologically hazardous and radiolabeled material is required.
What We Offer
Health & Wellness:
Medical, Dental, Vision Insurance
Life Insurance
Short & Long-Term Disability (multiple carriers)
Financial Benefits:
401(k) Retirement Plan
Paid Time Off (PTO)
Workplace Culture:
Employee Recognition Awards
Employee Resource Groups (ERGs)
Opportunities for professional growth and career advancement
Why Join Fortrea?
At Fortrea, you’ll:
Work on innovative early-phase clinical trials.
Collaborate in a high-impact, face-to-face clinical environment.
Contribute directly to the development of life-changing therapies.
Apply Now
To apply or learn more, visit: Fortrea Careers
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Equal Opportunity Employer
Fortrea is committed to diversity, inclusion, and equal opportunity in the workplace. Reasonable accommodations are available upon request. Learn more about our EEO & Accommodations.
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