• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits. • Provide mentoring and guidance to less experienced CRAs and site staff when needed. • Document site visit findings via written reports. • Assess, monitor, and train study site staff on protocol adherence as required. • Review study subject safety information and informed consent. • Conduct source document verification for compliance, patient safety, and veracity of data. • Review CRFs using paper or electronic data capture systems and assist sites with data query resolution. • Provide applicable updates for site related documentation for filing in the Trial Master File (TMF). • Ensure site compliance with IP receipt, accountability and return or destruction. • Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Conduct study initiation visits (SIVs) • Ensure compliance with obtaining informed consent and reporting potential safety-related events • Collaborate with top-tier colleagues from various backgrounds and specialties

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Involved in all stages of the clinical study, including identifying potential sites, performing various study start-up activities, training sites, managing site activities, and closing down research activities • Conduct study initiation visits (SIVs) • Ensure compliance with obtaining informed consent and adhering to regulatory requirements

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Conduct study initiation visits (SIVs) • Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements