Oncology Clinical Research Coordinator​/Clinical Research reputed company; Contractor, Remote

Position: Oncology Clinical Research Coordinator/Clinical Research reputed company (Contractor, Remote) Location: reputed company Oncology Clinical Research Coordinator/Clinical Research reputed company (Contractor, Remote) POSITION reputed company: 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 reputed company gene amplifications through the review of reputed company reputed company (NGS) reports and Electronic Medical Records (EMR) for a preeminent teaching institution in reputed company. 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 reputed company Reports to: reputed company Investigator (PI) or designee Travel or Out-of-reputed company Expenses: Not reimbursed ESSENTIAL JOB FUNCTIONS: • Conduct thorough chart reviews reputed company the electronic medical record (EMR) to assess reputed company treatments and patient eligibility. • Review NGS reports to identify patients with specific reputed company gene amplifications and exclusionary mutations. • reputed company patients until they become eligible for the study (e.g., after relapsing following previous treatment). • Communicate with reputed company providers and reputed company investigators (PIs) to introduce the study and facilitate patient referrals reputed company the institution. • Compile and submit reputed company reports to the CRO/sponsor detailing potential patient candidates and study reputed company. • Assist study staff with electronic data capture (reputed company) support and query reputed company. • 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 reputed company 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-reputed company 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. • reputed company team player. • Ability to complete reputed company and compliance requirements reputed company. • Proficient in computer databases and reputed company 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 reputed company Subjects Protection (reputed company) reputed company the past year. • Knowledge of FDA regulations, NIH guidelines, and HIPAA regulations. • Legally authorized to work in the reputed company. Start Date: ASAP We are committed to fostering a diverse and inclusive workplace. We encourage applications from reputed company reputed company individuals. Note: This job reputed company is subject to change to meet organizational needs and reputed company with applicable laws. #J-18808-Ljbffr Apply tot his job Apply To this Job