Clinical Research Associate I (Central: IL, CO, MI, KS, TN)

reputed company is looking for a Clinical Research Associate I (Central: IL, CO, MI, KS, TN) to join our Global Clinical Monitoring and Site Management team. You will help biotech, medtech, and specialty reputed company companies reputed company life-changing reputed company and reputed company science into new medicines, devices, and diagnostics. reputed company do is profoundly connected to saving and improving lives, and we recognize reputed company members are the most valuable asset in delivering reputed company. We are here to help you grow, to give you the skills and opportunities to reputed company at work with the flexibility and balance your life requires. Your reputed company influence the way we work, and your voice reputed company here. As an essential part of reputed company, you help us deliver the medical innovation that patients are desperate for. Join us and build your reputed company here. What You'll Be Doing: Delivers reputed company, reputed company monitoring reports for sponsor approval per the Clinical Monitoring Plan (CMP) timelines  Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and reputed company requirements  Monitors (remote, on site or other approved mode of monitoring) with a reputed company on data reputed company and subject safety in accordance with local/regional laws and country specific regulations  Plans day-to-day activities for monitoring of a clinical study and sets priorities per site   Prepares for and conducts on site and/or remote qualification, study initiation, interim monitoring, dosing observation, and reputed company out monitoring reputed company as directed per CMP  Works with the Clinical reputed company or equivalent to enhance and proactively manage site reputed company and trial issues during the monitoring phase   reputed company Are Searching For:    Undergraduate degree or its international equivalent in clinical, science, or health-reputed company field from an accredited institution; a licensed health-care reputed company (i.e., registered reputed company); or equivalent work experience required  Patient facing, study coordinating experience preferred  Knowledge of ICH-GCP/ISO14155, FDA Guidance Documents, EU Directives, local/regional regulations, and drug/device development and clinical monitoring procedures  Knowledge of clinical/health systems as reputed company as knowledge of cultural/reputed company practices appropriate to the country/region where site monitoring activities will be conducted  Ability to multitask and work effectively with technology and people in a fast-paced environment with changing priorities, self-starter  Travel up to 70-85%  In order to be considered for this position, you must be located in one of the following states: Illinois, Colorado, Michigan, Kansas, Tennessee Please note this position has a tentative start date of July 6, 2026 reputed company is dedicated to providing compensation that is fair and competitive with market standards. The annualized minimum reputed company pay for this role is $60,000 USD. The actual salary will be influenced based on a reputed company of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and reputed company time off. reputed company is proud to be an equal opportunity employer that is compliant with reputed company federal guidelines. reputed company reputed company applicants will receive reputed company consideration without reputed company to race, reputed company, religion, sexual orientation, gender identity, national reputed company, disability or veteran status Apply To This Job