<div>Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.<br /><br />The <strong>Clinical Research Coordinator (CRC)</strong> works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.  </div> <h2> Key Responsibilities </h2> <div><strong>Essential Job Duties: </strong>In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:</div><ul><li>Screening of patients for study enrollment; </li><li>Patient consents;</li><li>Patient follow-up visits;</li><li>Documenting in source clinic charts;</li><li>Entering data in EDC and answers queries;</li><li>Obtaining vital signs and ECGs;</li><li>May perform basic lab procedures per protocol, such as:  blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; </li><li>Requesting and tracking medical record requests;</li><li>Updating and maintaining logs, chart filings; </li><li>Maintaining &amp; ordering study specific supplies;]</li><li>Scheduling subjects for study visits and conducts appointment reminders;</li><li>Building/updating source as needed;</li><li>Conducting monitoring visits and resolves issues as needed in a timely manner;</li><li>Ensuring study related reports and patient results are reviewed by investigator in a timely manner;</li><li>Filing SAE/Deviation reports to Sponsor and IRB as needed;</li><li>Documenting and reporting adverse events;</li><li>Reporting non-compliance to appropriate staff in timely manner;</li><li>Maintaining positive and effective communication with clients and team members;</li><li>Always practicing ALCOAC principles with all documentation;</li><li>May assist with study recruitment, patient enrollment, and tracking as needed;</li><li>Maintaining confidentiality of patients, customers and company information, and;</li><li>Performing all other duties as requested or assigned.</li><li>Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;</li><li>Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;</li><li>May set up, train and maintain all technology needed for studies.</li></ul> <h2> Benefits </h2> 

Alcanza Clinical Research

PRN Traveling Clinical Research Coordinator Vaccine trial experience required Operations

Alcanza Clinical Research