Job Description A client is seeking a dedicated and detail-oriented Early Phase Research Nurse to join their team. In this role, you will be responsible for screening, enrolling, and following study subjects, ensuring rigorous protocol compliance, and providing close monitoring throughout their participation in the clinical trial. Your role will be critical in maintaining the integrity of the studies and ensuring the safety and well‑being of all participants. Day to Day Responsibilities Screen, enroll, and manage patients on early‑phase clinical trials (Phase 1) Coordinate all study‑related activities (labs, visits, treatments) according to strict protocols Monitor patients closely for safety, side effects, and adverse events Perform and support protocol‑specific activities (ex: timed labs, sample collection, study tracking tools) Work closely with physicians, research coordinators, and multidisciplinary teams Maintain detailed documentation and ensure compliance with regulatory guidelines Serve as a key point of contact for patients throughout the trial 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: Skills and Requirements Active RN license 5+ years of oncology experience At least 1 year of clinical research experienceExperience in or exposure to clinical trials (particularly early phase / phase 1 trials) Strong attention to detail and ability to follow strict protocols CERTIFICATIONS Must be eligible for ACRP (or have it already) Required to obtain ACRP within 6 months of meeting eligibility. Department reimburses this EDUCATION Associate degree; Bachelors preferred - Experience supporting Phase 1 or early drug development trials Research certification (or willingness to obtain within a defined timeframe) Previous experience in highly regulated or data‑driven environments Comfort working in more centralized or specialized clinical settings Bachelor's degree #J-18808-Ljbffr
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