Clinical Research Coordinator - Germantown, TN

## Clinical Research Coordinator - Germantown, TNApplylocations: Germantown, TNtime type: Part timeposted on: Posted Todayjob requisition id: R1550003# **Clinical Research Coordinator – Germantown, TN** **Work Set-Up:** On-site **Schedule:** Part-time, 24 hours per week### ### **About the Role**### We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance. Responsibilities also include working directly with consenting patients, conducting study visits, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures. Accurate and timely data entry will be an essential part of this role.### ### **About IQVIA**### IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.### ### **Key Responsibilities*** ### Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs.* ### Phlebotomy is required; pediatric experience is highly preferred.* ### Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.* ### Conduct patient consenting and perform study visits in accordance with study protocols.* ### Process laboratory samples and perform ABPM (ambulatory blood pressure monitor) procedures.* ### Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.* ### Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study.* ### Collect and accurately record clinical data in case report forms (CRFs); complete timely and high‐quality data entry.* ### Collaborate with investigators and monitors, addressing queries and ensuring data quality.* ### Act as a volunteer advocate and maintain a safe environment in accordance with Health and Safety policies.### **Qualifications*** ### High School Diploma or equivalent education and experience.* ### Minimum 1 year of relevant work experience in clinical research (preferred).* ### Working knowledge of clinical trials, GCP principles, and medical terminology.* ### Strong attention to detail and ability to establish effective working relationships.* ### Experience with CRIO is a plus.* ### **Experience with Allscripts/Altera EMR is a plus.**### ### ***Please note:** This position is not eligible for sponsorship.*### ### ### **#LI-CES #LI-DNP #LI-HCP #ONSITE**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 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. 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 is $35.00-$42.00 per hour. 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. #J-18808-Ljbffr