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

Job Title:

Clinical Research Coordinator Job Description The Clinical Research Coordinator is responsible for coordinating the initiation and activation of all new clinical trial protocols. This role involves developing study tools, reviewing patient charts, confirming protocol eligibility, and maintaining research records. Collaboration with Research Nurse Clinicians and physicians is crucial to ensure informed consent and accurate documentation. Additionally, the role includes grading adverse events, completing serious/unexpected adverse event forms, and liaising with study sponsors. Responsibilities Coordinate the initiation and activation of all new clinical trial protocols. Prepare study tools such as study binders, medication diaries, eligibility checklists, and flow sheets. Develop study tools using Oncore®, Excel®, and Word, including eligibility checklists, medication diaries, calendars, and flow sheets. 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. Maintain research records for all enrolled patients, including patient consent, eligibility, and corresponding source documents. Assist with grading adverse events using NCI common toxicity criteria or protocol-specific grading scales. Complete Serious/Unexpected Adverse Event forms as required by study sponsors and institutional guidelines. Provide regular reports to tumor study group members and Principal Investigator using Oncore®. Serve as study liaison with study sponsors, scheduling monitoring visits and conference calls. Essential Skills Minimum of 4 years of clinical research experience. Minimum of 4 years of oncology experience. Experience working in multiple EDC systems such as Medidata and Inform. Experience in data management, responsible for 60% of the role. Experience recruiting, screening, and consenting patients for clinical trials. Additional Skills & Qualifications Bachelor’s Degree minimum. Experience in blood processing. Experience from gynecology oncology group or nursing is acceptable. Work Environment The position requires on-site presence in the Bronx four times a week.