Clinical Research CoordinatorNJ Eye LLC is a private equity backed, independent, integrated eye care organization with its corporate headquarters in Union, New Jersey. The company has over 250 eye care professionals and business support roles across a growing network of over 17 eye care clinic locations, spanning New Jersey, with plans to affiliate with other eye care practices in New Jersey, New York, Connecticut, Pennsylvania, Delaware, Maryland, and nationwide.Role and Responsibilities:Leads recruitment efforts and screens potential patients for eligibility for studiesAbility to achieve enrollment targets on assigned studiesObtains informed consent from patients and conducts study visits for clinical trialsCreates Case Report FormsCompletes assessments on study subjects as per protocolDocuments study assessmentsEnters study data into EDC systemsCollects, processes, stores and ships lab specimens; documents lab procedures, lab results and follows up with patients and medical staff as necessaryCoordinates, monitors visits with CRAs for each trial to ensure accurate documentation; makes corrections to data as necessaryAssists during sponsor and FDA auditsResponsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisionsDocuments adverse events and notifies PI, sponsor and IRBAssumes test article accountabilityPossesses a sound and in-depth understanding of each protocol that has been assigned as a primary responsibilityMaintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR, and has IATA certificationTravels to investigator meetingsParticipates in weekly meetings with the research team, provides study metricsResponds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date mannerOther tasks as requiredQualifications:Education: Bachelor's degree preferably in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.Experience: 2+ years' relevant experience (e.g. research, clinical, interaction with study population, program coordination)Knowledge/Skills/Experience:Excellent Excel, Word, PowerPoint and reporting skillsExcellent interpersonal skills to deal effectively with patients, physicians, clinicians and administratorsExcellent organizational skills and self-management skills to independently manage work flowAbility to prioritizeMeticulous attention to detailKnowledge of medical terminologyKnowledge of good clinical practice, FDA, OHRP, HIPAA policiesAbility to use EMR data as a subject recruitment toolExperience using Microsoft Office Suite, and clinical research systems (CTMS, Regulatory)Certification through either ACRP or SoCRA highly preferredAt PRISM Vision Group, we believe great work deserves great rewards. Here's what you can expect when you join our team:Salary Range: $49,000.00 to $70,000 USDCompetitive Compensation Base salary, performance bonuses, and regular reviews.Health & Wellness Comprehensive medical, dental, and vision insurance; and wellness program.Retirement Planning 401(k) with company match.Generous Time Off Paid vacation, sick leave, and company holidays.Learning & Development career growth programs.Other Perks Commuter benefits, Voluntary Accident and Critical Illness plans, FSA/HSA and Dependent Care FSA. employee discounts, and more.NJ Eye LLC is an Equal Opportunity / Affirmative Action employer. Candidates are selected solely on the basis of legally permissible job-related criteria without regard to race, color, religion, sex, national origin, disability, marital status, or sexual orientation, in accordance with federal and state law.