Research Nurse Job at Insight Global, Nashville, TN

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  • Insight Global
  • Nashville, TN

Job Description

A client is seeking a detail-oriented and patient-focused Research Nurse to support oncology clinical trials in an outpatient setting. This role is responsible for coordinating patient participation in clinical studies from screening through follow-up while ensuring strict adherence to study protocols and regulatory requirements.
You will play a critical role in advancing oncology research by ensuring the successful execution of clinical trials. You will be responsible for screening, enrolling, documenting, and monitoring study subjects, ensuring strict protocol compliance and delivering exceptional patient care

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy:


Required Skills & Experience
• Active RN license
• 5+ years of oncology nursing experience
• At least 1 year of clinical research experience
• Experience or exposure to clinical trials (ideally early phase)

Soft skills:
- Flexibility to adapt across different clinic environments
- Team-oriented but also comfortable working independently
- Strong communication skills with patients and providers
- Able to manage multiple responsibilities simultaneously


Nice to Have Skills & Experience
• Experience supporting Phase 1 or early drug development trials
• ACRP certification OR eligibility to sit
• Strong understanding of GCP / regulatory environment
Experience with investigational drugs or PK studies


Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

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