• Serve as the primary internal and Sponsor contact for all Data Management questions, issues, and escalations related to data collection, cleaning, delivery, reconciliation, timelines, and database lock • Define, maintain, and communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams • Determine and document standard and study‑specific edit checks and data processing guidelines to ensure clean, high‑quality data • Collaborate with internal teams on study setup requirements, including demographics collection and visit schedule requirements • Lead the development, review, and finalization of data transfer requirements, including file specifications and approvals • Coordinate with SAS Programmers for data file creation, edit check development, and validation activities • Generate and deliver sample, routine, complete, and final data transfers in line with study timelines • Manage database lock activities with Sponsors to ensure data integrity and deliverable timelines are met • Act as the primary point of contact for Data Correction Requests (DCRs) and query escalation • Participate in the review and approval of Data Management components to ensure high‑quality study setups • Maintain complete and up‑to‑date Data Management documentation, including Data Management Plans, file specifications, data transfer agreements, data correction requests, and Sponsor communications • Identify out‑of‑scope requests and escalate to the Project Manager for Change Order processing • Conduct routine status meetings with Sponsors, CROs, and internal teams, including preparation of agendas and meeting minutes • Support monthly reporting activities by providing Data Management metrics as required • Deliver high levels of customer satisfaction by meeting commitments, timelines, and quality expectations

• Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. • Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing • May perform quality control of data entry • Provide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed. • Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders • May assist in building clinical databases • Conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database. • May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specifications • Responsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File. • Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed. • Review and query clinical trial data according to the Data Management Plan • Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM • Run patient and study level status and metric reporting • Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency • Coordinate SAE/AE reconciliation • Liaises with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables • May assist with SAS programming and quality control of SAS programs used in the Data Management department • Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders • May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project • Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities • May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings • May review Request for Proposals (RFP), proposals, provide project estimates • Provide leadership for cross-functional and organization-wide initiatives, where applicable • Trains and ensures that all data management project team members have been sufficiently trained • Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues • May present software demonstrations/trainings, department/company training sessions, present at project meetings • May require some travel • Perform other duties as assigned

• Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. • Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing. • May perform quality control of data entry. • Provide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed. • Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders. • May assist in building clinical databases. • Conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database. • May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specifications. • Responsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File. • Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed. • Review and query clinical trial data according to the Data Management Plan. • Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM. • Run patient and study level status and metric reporting. • Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency. • Coordinate SAE/AE reconciliation. • Liaises with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables. • May assist with SAS programming and quality control of SAS programs used in the Data Management department. • Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders. • May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project. • Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities. • May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings. • May review Request for Proposals (RFP), proposals, provide project estimates. • Provide leadership for cross-functional and organization-wide initiatives, where applicable. • Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues. • May present software demonstrations/trainings, department/company training sessions, present at project meetings. • May require some travel. • Perform other duties as assigned.

• Responsible and manages all aspects of the clinical trial data management process • Oversees and/or perform database development and testing • Primary Data Management (DM) contact for assigned projects • Oversee project data entry process • May perform quality control of data entry • Provide input, assesses and manage timelines • Develop CRF specifications from the clinical study protocol • Conduct database build UAT • Responsible for creating, revising, appropriate versioning and maintaining data management documentation • Train clinical research personnel • Review and query clinical trial data • Perform medical coding of medical terms