.Precision for Medicine is seeking an experienced Senior Clinical Data Associate to provide comprehensive data management support throughout all phases of the clinical trial data management process. Under direct supervision, you will ensure adherence to Standard Operating Procedures (SOPs), regulatory guidelines, and study-specific plans. This role encompasses a range of responsibilities, including data cleaning and reconciliations, database testing, quality control, and collaboration within a dynamic team environment. We can consider candidates working remotely in the following countries: Hungary, Romania, Poland, Slovakia, Serbia, Spain and UK.Position Summary:The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives: study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities.Essential functions of the job include but are not limited to:Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely mannerPerform data entry for paper-CRF studies, as neededPerform quality control of data entry. Provide input into timelines. Ensure that clinical data management deadlines are met with quality. May assess resource needs for assigned projects, as needed.Assist in developing CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholdersAssist in building clinical databases. Conduct database build UAT and maintain quality controlled database build documentation. May oversee overall quality of the clinical database.Assist in specifying requirements for all edit check types e.G., electronic, manual data review, edit checks, etc.Responsible for creating, revising, appropriate versioning and maintaining data management documentation.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 PlanPerform line listing data review based on the guidance provided by the sponsor and/or Lead DMRun 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 consistencyAssist with coordinating SAE/AE reconciliation.Assist with liaising with third-party vendors such as external data and EDC vendors in a project manager capacity in support of timelines and data-related deliverablesAssist with SAS programming and quality control of SAS programs used in the Data Management department
