Oncology Clinical Research Coordinator​/Clinical Research Nurse; Contractor, Remote

Position: Oncology Clinical Research Coordinator/Clinical Research Nurse (Contractor, Remote) Location: New York Oncology Clinical Research Coordinator/Clinical Research Nurse (Contractor, Remote) POSITION SUMMARY: We are seeking a dedicated Clinical Research Coordinator with oncology experience to support a multi-site oncology study. This role is essential in identifying patients with target gene amplifications through the review of Next-Generation Sequencing (NGS) reports and Electronic Medical Records (EMR) for a preeminent teaching institution in New York City. Type of Position: Contract, Full Time, Remote Study Duration: 12 months; 40 hours per week Location: Remote, must be available to support regular business hours for a site located in New York City Reports to: Principal Investigator (PI) or designee Travel or Out-of-pocket Expenses: Not reimbursed ESSENTIAL JOB FUNCTIONS: • Conduct thorough chart reviews within the electronic medical record (EMR) to assess current treatments and patient eligibility. • Review NGS reports to identify patients with specific target gene amplifications and exclusionary mutations. • Track patients until they become eligible for the study (e.g., after relapsing following previous treatment). • Communicate with healthcare providers and principal investigators (PIs) to introduce the study and facilitate patient referrals within the institution. • Compile and submit summary reports to the CRO/sponsor detailing potential patient candidates and study progress. • Assist study staff with electronic data capture (EDC) support and query resolution. • Collaborate with site staff and sponsors to ensure alignment with study objectives and timelines. • Other Duties as directed by the PI and or designee. SKILLS & ABILITIES: • Proficiency in navigating EMR and EDC systems. • Strong understanding of medical terminology and the ability to interpret research protocols. • Experience in reviewing oncology charts and assessing study eligibility. • Experience with reviewing and interpreting NGS reports is preferred but not required. • A background in a science-related field (e.g., biology, biomedical sciences) is highly desirable. • Strong organizational and communication skills, with the ability to work independently in a remote environment. • Willingness to learn and adapt to new concepts, with comprehensive training provided for NGS report review. • Strong verbal and written communication skills. • Collaborative team player. • Ability to complete onboarding and compliance requirements efficiently. • Proficient in computer databases and Microsoft Office Suite. EXPERIENCE AND EDUCATION: • Minimum of 2 years of experience in oncology as a Clinical Research Coordinator, Clinical Research Associate, or similar role. • Certification in GCP/ICH and Human Subjects Protection (CITI) within the past year. • Knowledge of FDA regulations, NIH guidelines, and HIPAA regulations. • Legally authorized to work in the United States. Start Date: ASAP We are committed to fostering a diverse and inclusive workplace. We encourage applications from all qualified individuals. Note: This job description is subject to change to meet organizational needs and comply with applicable laws. #J-18808-Ljbffr Apply tot his job