Job Title: Clinical Research Coordinator Job Description We are seeking a dedicated Clinical Research Coordinator to join our growing team. This role involves coordinating the day-to-day operations of oncology clinical trials, ensuring compliance with study protocols and regulatory guidelines. The ideal candidate will have a strong background in clinical research, specifically in oncology, and possess excellent organizational and communication skills. Responsibilities + Coordinate the day-to-day operations of oncology clinical trials, ensuring compliance with study protocols and regulatory guidelines. + Serve as the primary point of contact for study participants, ensuring their understanding of the trial, addressing their concerns, and providing updates on study progress. + Collect, record, and maintain accurate study data in accordance with the study protocol and regulatory requirements. + Ensure compliance with local, state, and federal regulations, including submission of documents to Institutional Review Boards (IRBs) and other regulatory bodies. + Work closely with the Principal Investigator (PI), study sponsors, clinical research associates (CRAs), and other stakeholders to ensure smooth study operations. + Track patient progress and ensure adherence to the clinical trial schedule. + Assist in educating patients and their families about the clinical trial process. + Maintain thorough and accurate records of all study-related activities. Essential Skills + Health care + Oncology nursing + Oncology + Patient education + Epic + Electronic health record + Patient recruitment + Regulatory compliance + Clinical research coordination (CRC) + Project management + Data entry + Clinical study conduct + Phlebotomy + Pre-screening patients + Data management Additional Skills & Qualifications + Bachelor’s degree in Life Sciences, Nursing, or related field required. + Certification in Clinical Research (CCRP or CCRC) preferred. + At least 2 years of experience in clinical research, with mandatory experience in oncology. + Knowledge of Good Clinical Practice (GCP) and regulatory requirements. + Proficient in data management and documentation practices. + Excellent communication skills, both written and verbal. + Strong organizational and multitasking abilities. + Attention to detail and ability to work independently as well as part of a team. + Familiarity with clinical trial software and data management systems. Work Environment This is a permanent, on-site position with a typical work schedule of Monday to Friday, 8:00 AM to 5:00 PM. The role is based across three locations: Hinsdale, New Lenox, and Morris. The clinic is experiencing growth in both research and patient enrollment, offering a family-like environment and opportunities for advancement within the growing research portfolio. Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for more information. Pay and Benefits The pay range for this position is $75000.00 - $85000.00/yr. They will provide a package with PTO, Medical and eye etc. Investment vehicles are available.......... Workplace Type This is a fully onsite position in Hinsdale,IL. Application Deadline This position is anticipated to close on Mar 6, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.