Clinical Oncology Nurse Coordinator

Primary Responsibilities Performs project analysis and administration by: Assist oncology team members on protocol documents, imaging manuals, clinical data transfer plans and business requirements Pre-read and pre-quant cases for oncologist to increase margin and efficiency. Participate in project meetings, conference calls, training sessions and bid defenses Act as a liaison with cross-functional team members to provide scientific support Investigate study needs/issues and work directly with other teams to identify solutions Contributes to the requests for proposal (RFP) process with business development and contracts & proposals teams Contribute to the software validation, user acceptance testing and support of client application build Research and respond to both client and internal department queries Assist in training and supervising team members on the oncology QC process and assist with re-training efforts as necessary Act as the team lead for process improvement initiatives in support of clinical data workflows with sponsor, internal teams members and external readers Supports Manager by: Monitoring internal data flow to ensure completion of tasks with agreed upon time frames Assist with the development of operational strategies for oncology clinical data workflows and read criteria Consult with other departments and sponsors on response criteria and read methodology Assist in configuring client and project specific data specifications, forms, mapping, etc. Create and edit project presentations as needed Assist with on-boarding external oncologists for read projects Execute the delegation of various team task assignments Assist with client data transfer schedule for reader assignment and prioritization Provides team leadership by: Leading by example with professional and collaborative conduct Developing and delivering training to multiple departments Establishing team performance expectations and guidelines Secondary Responsibilities Manages assigned department initiatives by: Research, evaluate and become Subject Matter Expert (SME) in assigned disease Research and implement measures to streamline processes Maintain quality service and departmental standards by: Reading, understanding, and adhering to organizational standard operating procedures (SOPs) Contribute to team effort by: Working with internal staff to identify and resolve issues Collaborate with departmental team members to achieve quality results Assist with ad hoc tasks Maintain technical and industry knowledge by: Attending and participating in applicable company-sponsored training Participating in documents associated to the various disease related studies and participate in the collaboration of applying new and modified read criteria. Qualifications: Education Registered Nurse with BSN with Oncology experience Experience 3 years’ experience working with clinical trials and/or within pharmaceutical environment with oncology related activities required Experience with multi-modality clinical projects management is a plus Experience with medical imaging software a plus Experience working with computer software including the MS Office suite Additional skill set: Ability to work in group setting and independently Ability to adjust to changing priorities and execute on multiple tasks as needed Ability to organize and prioritize assigned tasks to meet established schedules, timelines, or deadlines Strong interpersonal and communication skills (both verbal and written) Excellent attention to detail and meticulous work Ability to maintain a professional and positive attitude Working conditions: Travel: 0-5% Lifting: 0-15 lbs Other: Computer work for long periods of time EEO Statement Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic This position description should not be deemed all inclusive. Additional requirements and expectations may be assigned. At all times, employees are expected to adhere to company policies and company SOPs. Clario Privacy Policy Clario delivers the leading endpoint technology solutions for clinical trials. Through experience gained from over 19,000 clinical trials delivered in support of 870 regulatory approvals, Clario fuses scientific expertise and global scale into the broadest endpoint technology platform to enable pharmaceutical, biotech and medical device partners to transform lives. Through Trial Anywhere™, Clario has mastered the ability to generate rich evidence across all trial models: decentralized, hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe and Asia Pacific, Clario’s global team of science, technology and operational experts has been delivering the richest clinical evidence for nearly 50 years.