• Participate in study feasibility assessments, and site selection processes • Assist in the preparation and review of essential documents such as informed consent forms (ICFs) and study manuals • Conduct site qualification, site initiation, interim monitoring, and close-out visits • Regularly review Investigator Site Files (ISF) to assist in maintaining site audit readiness • Perform routine site communication, including resolving site issues and providing protocol training as necessary • Contribute to development and delivery of CRA training materials • Mentor and support junior CRAs and newly onboarded CRAs • Review study documents including the Clinical Monitoring Plan and Investigator Site File documents • Participate in trial risk management meetings and procedures • Monitor and review clinical data to ensure accuracy, completeness, and timeliness • Work closely with data management teams to resolve data discrepancies and ensure data integrity throughout the trial • Assist in the preparation of regulatory submissions and support inspections/audits as needed • Foster strong relationships with investigators, study coordinators, and other key stakeholders • Provide regular updates to internal teams and management regarding study progress, issues, and resolutions

• Participate in study feasibility assessments, and site selection processes • Assist in the preparation and review of essential documents such as informed consent forms (ICFs) and study manuals • Conduct site qualification, site initiation, interim monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines • Regularly review Investigator Site Files (ISF) to assist in maintaining site audit readiness • Perform routine site communication, including resolving site issues and providing protocol training as necessary • Contribute to development and delivery of CRA training materials • Mentor and support junior CRAs and newly onboarded CRAs • Review study documents including the Clinical Monitoring Plan and Investigator Site File documents • Participate in trial risk management meetings and procedures • Identify, develop and implement process improvement initiatives to enhance monitoring quality and mitigate trial risks • Monitor and review clinical data to ensure accuracy, completeness, and timeliness • Work closely with data management teams to resolve data discrepancies and ensure data integrity throughout the trial • Assist in the preparation of regulatory submissions and support inspections/audits as needed • Ensure that all clinical trial activities are conducted in accordance with applicable regulatory requirements and internal procedures • Foster strong relationships with investigators, study coordinators, and other key stakeholders • Provide regular updates to internal teams and management regarding study progress, issues, and resolutions.

• Coordinates investigator/ site feasibility and identification process, as well as study startup. • Monitors project timelines and patient enrollment, implements respective corrective and preventive measures. • Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region. • Manages Monitors in the query resolution process, including Central Monitoring observations. • Coordinates safety information flow and protocol/process deviation reporting. • Performs clinical supplies management with vendors on a country and regional level. • Ensures study-specific and corporate tracking systems are updated in a timely manner. • Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager. • Coordinates planning of supervised monitoring visits and conducts the visits. • Manages the project team in site contracting and payments. • Leads project team calls on a country level as well as provides status updates and reports to Regional Lead/ Project Manager. • Ensures ongoing evaluation of data integrity and compliance at a country/regional level. • Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level. • Oversees project team in CAPA development and implementation. • Coordinates project team in process deviations review, management and reporting. • Conducts initial training and authorization monitoring visits for Monitors and acts as a mentor for newly promoted Lead CRAs. • Provides project-specific training and prepares training materials for the project team under supervision of a Project Manager and Regional Project Lead. • Delivers trainings and presentations at Investigator Meetings. • Prepares, conducts and reports site selection, initiation, routine monitoring and closeout visits. • Ensures that subject recruitment targets and project timelines are properly defined, communicated, recorded, and met at site level. • Ensures accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations. • Supervises source data verification and follows up on data queries at site level in the country/region; reviews and manages study risks on a site level. • Ensures proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on a country/region level. • Reviews essential study documents and supervises reconciliation of study Investigator Site File (ISF) / TMF at site level and country/region level. • Ensures data integrity and compliance at a site level. • Supervises Site Management Associates in the flow of documents and laboratory supplies between the site and the Central/ Regional Lab/ Central Reviewer. • Conducts project-specific training of site Investigators. • Supports preparation of draft regulatory and ethics committee submission packages.

• Coordinates investigator/ site feasibility and identification process, as well as study startup. • Monitors project timelines and patient enrollment, implements respective corrective and preventive measures. • Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region. • Manages Monitors in the query resolution process, including Central Monitoring observations. • Coordinates safety information flow and protocol/process deviation reporting. • Performs clinical supplies management with vendors on a country and regional level. • Ensures study-specific and corporate tracking systems are updated in a timely manner. • Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager. • Coordinates planning of supervised monitoring visits and conducts the visits. • Manages the project team in site contracting and payments. • Leads project team calls on a country level as well as provides status updates and reports to Regional Lead/ Project Manager. • Ensures ongoing evaluation of data integrity and compliance at a country/regional level. • Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level. • Oversees project team in CAPA development and implementation. • Coordinates project team in process deviations review, management and reporting. • Conducts initial training and authorization monitoring visits for Monitors and acts as a mentor for newly promoted Lead CRAs. • Provides project-specific training and prepares training materials for the project team under supervision of a Project Manager and Regional Project Lead. • Delivers trainings and presentations at Investigator Meetings. • Prepares, conducts and reports site selection, initiation, routine monitoring and closeout visits. • Ensures that subject recruitment targets and project timelines are properly defined, communicated, recorded, and met at site level. • Ensures accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations. • Supervises source data verification and follows up on data queries at site level in the country/region; reviews and manages study risks on a site level. • Ensures proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on a country/region level. • Reviews essential study documents and supervises reconciliation of study Investigator Site File (ISF) / TMF at site level and country/region level. • Ensures data integrity and compliance at a site level. • Supervises Site Management Associates in the flow of documents and laboratory supplies between the site and the Central/ Regional Lab/ Central Reviewer. • Conducts project-specific training of site Investigators. • Supports preparation of draft regulatory and ethics committee submission packages.