About Valley Medical Research Valley Medical Research is an independent, physician-led clinical research site in Dayton, Ohio, with more than 20 years of experience conducting Phase [II-IV] clinical trials for pharmaceutical sponsors and CROs. We have completed over 300 studies in cardiovascular disease, neurology and Alzheimer's disease, arthritis, metabolic disease and diabetes, and vaccines, and have built long-standing sponsor relationships on clean data and on-time enrollment. We are owner-operated and deliberately sized: small enough that every coordinator knows every study, and large enough to run a steady pipeline of trials year-round. Coordinators here are not siloed into one task. They own their studies end to end and learn the full lifecycle of a trial across multiple therapeutic areas. The Role We are hiring an experienced Clinical Research Coordinator to manage assigned studies from start-up through close-out. You will work directly with our principal investigator, sponsors, CROs, and study participants, and will be expected to run your studies independently from day one. Responsibilities Coordinating all study activities in compliance with the protocol, ICH-GCP, FDA regulations, and site SOPs Preparing and maintaining regulatory documents and IRB submissions, including initial submissions, amendments, and continuing reviews Recruiting, pre-screening, and enrolling participants, and conducting the informed consent process Scheduling and conducting study visits, including vitals, ECGs, phlebotomy, and specimen processing and shipping Maintaining accurate source documentation and entering data into EDC systems in a timely manner Resolving data queries and preparing for and supporting monitor visits and audits Managing investigational product accountability and study supplies Tracking adverse events and reporting them to sponsors and the IRB per protocol requirements Communicating with sponsors and CROs on study status, enrollment, and issues Attending investigator meetings and sponsor training as needed, with occasional travel Requirements Minimum [1] year of experience as a Clinical Research Coordinator at a research site Active RN, LPN, or Medical Assistant credential Proficiency in phlebotomy, vitals, and ECG administration Current GCP training; ACRP (CCRC) or SOCRA (CCRP) certification, or willingness to obtain within [12] months Working knowledge of

ICH-GCP, FDA

regulations, and IRB processes Experience with EDC systems and electronic regulatory or CTMS platforms Valid driver's license and ability to travel occasionally for investigator meetings Strong organization, attention to detail, and written and verbal communication skills Comfortable working directly with patients and physicians Join us in advancing healthcare through meticulous research coordination that upholds the highest standards of clinical excellence! To Apply Send your resume to mpatelmd@ymail.com or apply through LinkedIn. [Valley Medical Research is an equal opportunity employer.]

Pay:

$25.00 - $34.00 per hour Expected hours: 30.0 - 40.0 per week

Benefits:

Health insurance Paid time off Application Question(s): Do you have any experience in clinical trials? How many years of clinical trial experience do you have? Are you certified as an LPN, RN, or CCMA?

Work Location:

In person