Carlos Sampson

Clinical Research Coordinator @Alcanza Clinical Research

US

Screening of patients for study enrollment. Patient consents. Patient follow-up visits. Documenting in source clinic charts. Entering data in EDC and answers queries. Obtaining vital signs and ECGs. 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. Requesting and tracking medical record requests. Updating and maintaining logs, chart filings. Maintaining & ordering specific supplies. Scheduling subjects for study visits and conducting appointment reminders. Building/updating the source as needed. Conducting monitoring visits and resolving issues as needed in a timely manner. Ensuring study related reports and patient results are reviewed by investigators in a timely manner. Filing SAE/Deviation reports to Sponsor and IRB as needed. Documenting and reporting adverse events. Reporting non-compliance to appropriate staff in a timely manner. Maintaining positive and effective communication with clients and team members. Always practicing ALCOAC principles with all documentation. May assist with study recruitment, patient enrollment, and tracking as needed. Maintaining confidentiality of patients, customers and company information, and. Performing all other duties as requested or assigned. Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc. Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed. May set up, train and maintain all technology needed for studies.