.our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world's most challenging health concerns. Our clinical research team, who powers our ppd® clinical research portfolio, are part of our leading global contract research organization (cro).description - externalprepares and analyzes clinical trial patient datasets, such as laboratory data, vital signs data, tumor response data, imaging data, quality of life and well-being questionnaire data, or adverse events data, for clinical research purposes.increases knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry by working closely with mentors, attending presentation / teaching events, and contributing to other general department documents and policies by assisting mentors with implementing best practice documents and articles.rsm-central performs related activities on assigned project(s) in accordance with the approved protocol, ich-gcp guidelines, applicable regulations and crg sops. In addition, reviews study data from various sources remotely. They develop collaborative relationships with different stakeholders as applicable.reviews ad-hoc clinical listings review, tracks and trends violations and deviations, site status, enrollment, crf status and sae follow up.provides trial status tracking and progress update reports to study manager.participates in the investigator payment process, if applicable.assists in ensuring audit ready files and complying with ctms and etmf data stewardship. Contributes to company, client, and federal/local regulatory requirements/audit responses.*qualifications - external*- bachelor's degree in life science-related field, it, engineer, biostatistics or programing.- prior clinical research experience 0-1 year as well as knowledge of clinical monitoring through classwork/training that provides the required knowledge skills and abilities. In some cases, previous experience in a clinical environment where experience is gained in clinical trials, data management