Job Description

Overview Join to apply for the Clinical Research Coordinator role at Emerson Clinical Research Institute . Our clinical research company is hiring for a full-time position in New Jersey. The ideal candidate will have prior medical assistant or clinical trial experience, phlebotomy skills, be fully bilingual in Spanish and English, and be committed to working with diverse patients. Responsibilities Conduct IRB-approved clinical trial activities: participant identification, screening, randomization, enrollment, and conducting clinic visits. Perform and assist with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc. Coordinate study visits, follow-ups, and reminder calls with study participants. Data entry of case report forms and study visits across study platforms within 24 hours of data collection. Maintain high attention to detail for data integrity, regulatory compliance, site visits, study setup and maintenance, and protocol adherence. Communicate effectively to foster relationships between the research team, PIs, Sponsors, Monitors, and others. Stay focused across multiple protocols, resolve and submit IRB responses and audit findings, track AE/SAE events, and maintain eSource materials. Support recruitment directives, meet financial goals, and participate in overall study operations. Promote the mission of ECRI as an Integrated Site Network, delivering service to clinical trial partners. Meet and strive to exceed priorities as discussed with supervision; manage daily site operations; comply with SOPs and regulatory requirements. Collaborate with pharma sponsor clinical research professionals on regulatory document processing and submission; assist in development of case report forms. Engage in other clinical research activities as assigned; manage training records for ECRI staff. Minimum Requirements Bilingual in English and Spanish; able to recruit and consent patients in both languages. 4-year degree or equivalent in Biology, Pharmacology, or a health-related field preferred. Ability to adapt to a constantly changing environment. Minimum 1–2 years of experience in clinical research trials. Strong interpersonal and communication skills with a customer-service focus. CITI training completed before start date. Excellent organizational and time-management skills; ability to conduct independent research activities; self-motivated and deadline-driven. Legal authorization to work in the US. Working conditions Direct patient contact and phlebotomy procedures as needed; universal precautions required to handle biological samples. Occasional travel, including air travel, to attend leadership and investigator meetings. On-site position only; remote work is not available. What We Offer Competitive compensation, 401(k) with company match Clear career pathway for advancement Health and dental insurance plans Generous PTO and paid holidays Paid sick days Company Description ECRI is a clinical research institute with headquarters in Washington, DC, and sites in Chicago and New Jersey. ECRI has been recognized by Merck as a Diversity Center of Excellence and works with multiple pharma sponsors. Our focus is on increasing patient access to research trials in diverse communities, supporting physicians with enhanced care options, and delivering superior enrollment metrics to sponsors to improve patient outcomes. #J-18808-Ljbffr Emerson Clinical Research Institute

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