Part -Time Clinical Research Coordinator

Optum NY/NJ, is seeking a Part -Time Clinical Research Coordinator to join our team in Mount Kisco, NY. Optum is a clinician-led care organization that is changing the way clinicians work and live. As a member of the Optum Care Delivery team, you'll be an integral part of our vision to make healthcare better for everyone. At Optum, you'll have the clinical resources, data and support of a global organization behind you so you can help your patients live healthier lives. We believe you deserve an exceptional career, and will empower you to live your best life at work and at home. Experience the fulfillment of advancing the health of your community with the excitement of contributing new practice ideas and initiatives that could help improve care for millions of patients across the country. Because together, we have the power to make health care better for everyone. Join us and discover how rewarding medicine can be while Caring. Connecting. Growing together. Optum is seeking a Part-Time Clinical Research Coordinator to support oncology care teams and guide patients through clinical research activities. Schedule : This is a 20-hour work week, Monday through Friday between the hours of 8;30am to 5:00 pm. The schedule will be determined by the hiring manager upon hire. Location: 90 South Bedford Road, Mount Kisco, 10549 Will travel to other treating site locations: 30 Columbia Street Poughkeepsie, NY 12601 600 Westage Business Center Drive, Fishkill, NY 12524 1400 Old Country road, Westbury, NY 11590 Primary Responsibilities: Fully comprehend study protocols and ensure all procedures and assessments (including screening and end of treatment) are carried out per protocol specifications. Collect and document accurate and verifiable data. Maintain protocol, GCP, ICH compliance. Adhere to organizational SOPs. Be present at all required study visits to assist the investigator with adherence to the protocol and collect all data for visit. Assist the investigator, onsite staff, and patient in scheduling the study procedures and appointments (scans, EKGs, labs, any outside exams). Assist in carrying out administrative procedures for the consent, enrolling and randomization process. Prepare, process, and ship laboratory specimens as required per protocol. Complete study synopsis notes and enter data into the study-specified database, electronic data capture (EDC). Collect complete medical and disease history via chart review and patient interview. Collect current medication list, subject health information, and occurrence of adverse events. Plan the subject calendar in advance for cycles and visits based on the schedule of assessments, including ability to efficiently manage your and the subject's time, and to think ahead for the next visit. Assist the pharmacy/corporate office in provision and collection of study medications and performing drug accountability. Participate in monitor visits as needed. Prescreen EMRs for potential patients to enroll in studies. Communicate effectively with physicians, multi-disciplinary teams, patients, sponsors, CROs, and other team members. Prepare and be available for monthly recruitment calls with sponsors regarding prescreening updates, patient enrollment projections, barriers to recruitment, elaborate on inclusion/exclusion criteria difficult to meet, etc . Prepare and be responsible for database locks that occur every 3 months for all active studies. Turnaround time is within 24 hours to respond to urgent emails. Attend investigator meetings for all active studies. Performs other duties as assigned What are the reasons to consider working for UnitedHealth Group? Put it all together - competitive base pay, a full and comprehensive benefit program, performance rewards, and a management team who demonstrates their commitment to your success. Some of our offerings include: Paid Time Off which you start to accrue with your first pay period plus 8 Paid Holidays Medical Plan options along with