Sr. Clinical Research Coordinator RO Position Available In Bronx, New York

Job Title:

Clinical Research Coordinator Job Description The Clinical Research Coordinator will play a pivotal role in coordinating the initiation and activation of new clinical trial protocols, ensuring all necessary study tools are prepared and utilized effectively. This position requires a robust background in data management and clinical research, with a strong focus on oncology trials. Responsibilities Coordinate the initiation and activation of all new clinical trial protocols. Prepare study tools including study binders, medication diaries, eligibility checklists, and flow sheets using Oncore®, Excel®, and Word. Collaborate with the Research Nurse Clinician and/or physician to review patients’ charts and medical history to confirm protocol eligibility and obtain necessary source documents. Ensure IRB-approved informed consent forms are obtained, signed, and correctly filed in medical records, providing copies to patients. Maintain comprehensive research records for all patients enrolled in studies, including consent, eligibility, Case Report Forms, and registration confirmations. Assist with grading adverse events and complete Serious/Unexpected Adverse Event forms as required by study sponsors and institutional guidelines. Provide regular reports to tumor study group members and Principal Investigators on assigned studies using Oncore®. Serve as a liaison with study sponsors, scheduling monitoring visits and conference calls, and respond accurately and timely to sponsors’ queries. Essential Skills Minimum of 4 years of clinical research experience. At least 4 years of oncology experience. Experience working in multiple EDC systems, specifically Medidata and Inform. Strong background in data management, with 60% of the role focusing on data coordination. Experience in recruiting, screening, and consenting patients for clinical trials. Blood processing experience is required. Additional Skills & Qualifications Bachelor’s Degree is required. Experience can come from clinical research, school, or nursing backgrounds, particularly in gynecology oncology groups. Work Environment This position requires onsite work in the Bronx four days a week. The work involves collaboration with tumor study group members, Principal Investigators, and study sponsors, utilizing multiple EDC systems in a clinical setting.