Medical Assistant - Research Assistant

<div class="content-intro"><p>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</p></div><p>&nbsp;</p> <p data-start="167" data-end="247">&nbsp;</p> <div class="ql-block" data-block-id="block-exfc11cw_A">📍&nbsp;<strong>Pikesville, MD</strong></div> <div class="ql-block" data-block-id="block-qFsrSOZK5Z">🏥&nbsp;<strong>PharmaSite Research</strong></div> <div class="ql-block" data-block-id="block-Ez0pTXSu9i">🕒&nbsp;<strong>Full-Time | Monday through Friday | 9:00am - 5:00pm</strong></div> <h3 data-section-id="s6vv15" data-start="249" data-end="298">&nbsp;</h3> <h3 data-section-id="s6vv15" data-start="249" data-end="298">Launch Your Career in Healthcare &amp; Research</h3> <p data-start="268" data-end="528">Are you a recent graduate looking to gain hands-on experience in healthcare or clinical research? This is an exciting opportunity to work directly with patients, support clinical trials, and build real-world skills alongside experienced research professionals.</p> <p data-start="530" data-end="935">As a&nbsp;<strong data-start="535" data-end="566">Clinical Research Assistant</strong>, you’ll play a key role in supporting study visits, interacting with patients, and ensuring research is conducted safely and accurately. Whether you're planning a future as a Clinical Research Coordinator, healthcare provider, or pursuing advanced education, this role provides a strong foundation and meaningful exposure to a fast-paced, patient-centered environment.</p> <p data-start="299" data-end="612">&nbsp;</p> <hr data-start="951" data-end="954"> <h3 data-section-id="xti9y5" data-start="956" data-end="976">Responsibilities:</h3> <ul> <li>Study Preparation <ul> <li>Prepare and maintain study documents, including source charts, study binders, regulatory binders, and laboratory kits.</li> <li>Schedule and confirm subject appointments, including ancillary visits such as diagnostic imaging and vendor-related services.</li> <li>Understand study protocols, inclusion/exclusion criteria, and regulatory requirements, ensuring compliance with FDA, Sponsor, and Go