WHY VITALIEF? Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic.  Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions.  Reasons to Work for Vitalief: + Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees. + We give everyone a seat at the table – we encourage innovation. + We’re committed to our employees – you are encouraged and mentored by the talented Vitalief team to achieve full potential. + “Life/Work” balance that includes 20 PTO (Paid Time Off) days plus 9 paid Holidays annually. + Other benefits include Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from. Salary Range:  $60,000 to $70,000 annually Work Location:  Work is 5 days per week on-site in Newark, NJ. Job Responsibilities: + Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you will be responsible for performing a wide variety of tasks to ensure successful Oncology related clinical trials. + Manage eligibility check lists, perform patient screening/consenting (informed consent), patient activation and managing patient care (patient retention). + Assist with monitoring patient visits. + Track deviations and documenting SAEs (serious adverse events). + Ship specimens to central labs or research labs. + Track data queries and prepare data for an upcoming audit. + Work collaboratively with all team members (i.e., physicians, nurses, hospital, and laboratory staff) to ensure that services are coordinated and delivered to patients in a timely manner. Required Skills: + Minimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance and data management. + Bachelor’s Degree required. + Any experience in Oncology and/or working on complex clinical trials is a plus. + Ability to work on 12 to 15 concurrent trials – must have strong organizational and prioritization skills. + The keys to success in this role are your ability to demonstrate your versatility, “can do” attitude, and adaptability. + Considerable understanding of Good Clinical Practice (GCP) guidelines. + Experience in preparation of documents for submission to the Institutional Review Board (IRB), continuing reviews, and submission of amendments and modifications. + Experience ensuring Serious Adverse Events (SAEs) are completed and reported to the QA Manager and sponsor, if necessary, within reporting deadlines outlined in the protocol. + Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus. PHYSICAL DEMANDS: Standing, sitting, walking, talking, hearing, and visual perception. Lifting up to 25lbs. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNI   Powered by JazzHR