• Contribute to construction and QC of longitudinal electronic health record (EHR) analytic files using structured data • Conduct descriptive analyses of patient demographics, lab values, medication use, and clinical characteristics • Summarize data availability, follow-up patterns, and measurement frequency across CKD subgroups • Support feasibility assessments by generating counts, proportions, and distributional summaries • Produce clean, well-documented analytic code and contribute to draft tables and figures • Participate in biweekly internal team meetings and client meetings, and contribute to written deliverables

• Conduct deep-dive investigative research into applicant information by cross-referencing multiple internal and external data sources to verify business legitimacy and financial health • Analyze discrepancies in applicant documentation and independently resolve complex verification issues by applying sound critical thinking and judgment • Maintain high standards of accuracy and thoroughness while meeting daily production benchmarks in a fast-paced fintech environment • Partner with underwriting and partner relations teams to provide clear, actionable insights derived from your research, supporting Credibly’s goal of accelerated, right-sized capital solutions • Identify and document patterns of risk or process inefficiencies to support platform enhancements and improve data quality

• Monitoring and Management of Investigator Sites • Conducts source data verification (SDV) and ensure clinical trials data are submitted to data management in a timely fashion • Identifies issues that may impact on the conduct of the study and ensure appropriate closure of all issues • Proactively manages a greater investigator site workload commensurate with experience, so that studies are run efficiently, and key study objectives are met • Ensures studies are run in line with ICH/GCP, local laws and Client Standard Operating Procedures (SOPs) and procedures • Ensures patient safety is maintained and all safety issues are reported correctly according to all relevant local and international regulatory requirements • Informs the Principal Investigator (PI) and site staff of all issues • Agrees and develops corrective and preventative actions with PI and site personnel to close all open issues • Responsible for all aspects of site management from collaboration on site selection to study closeout • Trains site staff on the protocol, protocol amendments and Client processes • Understands the product, the protocol, and the therapy area in sufficient detail to be able to have appropriate discussions with the investigator team • Interacts with health care professionals in a manner, which enhances Client’s credibility with the customer • Ensures that data monitored meets target quality standards • Ensures that data is entered into Client systems in a timely manner • Reports on progress of all studies at the investigational site after each visit to ensure that all relevant personnel are aware of progress against plan and any issues that have occurred • Ensures all issues are correctly identified and catalogued • Proactively manages issues to appropriate closure • Maintains accurate site-level information on corporate clinical trials registry • Obtains critical information to enable generation of Investigator Initiation Package (IIP) documentation • Assists Clinical Trial Assistant (CTA) in gathering IIP documentation where required to ensure timely site set up • Maintains the Site Master File (SMF) and SMF log • Ensures Electronic Library and Records Archive (ELARA) and/or Client Trial Master File (TMF) is complete and accurate • QC relevant documents in ELARA and/or TMF in a timely manner • Generates site monitoring reports • Maintains all appropriate monitoring logs • Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required • Maintains a working knowledge of and complies with Parexel processes, ICH- GCPs and other applicable requirements

• You will be dedicated to a single client • You will be responsible for all site management and supervisory activities in the assigned oncology studies. • You will work with industry leaders and subject matter experts. • You will have the opportunity to mentor junior CRAs. • You will work with world-class technology. • You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.