Clinical Research Associate, Sponsor Dedicated

Durham, North Carolina, United States of America Aurora, Illinois, United States San Fernando, California, United States Clinton, Missouri, United States Mansfield, Ohio, United States Santa Cruz, California, United States Santa Fe, New Mexico, United States South Shore, Illinois, United States Elk Grove, California, United States Hudson, Ohio, United States Englewood, Colorado, United States Bellingham, Washington, United States Marysville, Washington, United States Overland Park, KS, United States of America Evanston, Wyoming, United States La Habra, California, United States Prescott, Arizona, United States Westchester, New York, United States Mount Vernon, Illinois, United States Warren, Ohio, United States of America Linden, New Jersey, United States Fremont, California, United States Del Mar, California, United States Lake Tahoe, California, United States Northfield, New Jersey, United States Fort Pierce, Florida, United States Wilkes Barre, Pennsylvania, United States Camden, New Jersey, United States Lancaster, California, United States Clarksville, Tennessee, United States Adair, Iowa, United States Fort Collins, Colorado, United States Breckenridge, Colorado, United States Littleton, Colorado, United States Liverpool, New York, United States Ft Lauderdale, Florida, United States Springfield, Ohio, United States Long Island, New York, United States Gloucester, Virginia, United States West Point, Virginia, United States O'Fallon, Illinois, United States Cheyenne, Wyoming, United States Manhattan, New York, United States New City, New York, United States Parsippany, New Jersey, United States of America Queens, New York, United States New York City, New York, United States Escondido, California, United States Oak Brook, Illinois, United States Merritt Island, Florida, United States El Cajon, California, United States Ontario, California, United States Afton, Wyoming, United States Abilene, Texas, United States Orangevale, California, United States Abingdon, Virginia, United States Orland Park, Illinois, United States Shenandoah, Texas, United States Akron, Ohio, United States Paradise Valley, Arizona, United States Newark, Delaware, United States Hollywood, Florida, United States Port Saint Lucie, Florida, United States Lawton, Oklahoma, United States Portland, Oregon, United States Chino Hills, California, United States Belmar, New Jersey, United States Sonora, California, United States Berkley, California, United States Springfield, Massachusetts, United States Springfield, Missouri, United States San Jose, California, United States Beverly Hills, California, United States Melbourne, Florida, United States Colorado Springs, Colorado, United States St. Petersburg, Florida, United States Panama City, Florida, United States Redondo Beach, California, United States Crystal Lake, Illinois, United States Rochester, New York, United States Ada, Oklahoma, United States Kansas City, Missouri, United States Ainsworth, Nebraska, United States Carlsbad, CA, United States of America Denver , Colorado, United States Full time To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Bachelor's Degree Degree in scientific discipline or health care preferred. Requires at least 2 years of year of on-site monitoring experience. Equivalent combination of education, training and experience may be accepted in lieu of degree. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $71,900.00 - $189,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr