The Senior Data Manager   PRECISION LIFE SCIENCES The Senior Data Manager brings an advanced understanding of the clinical data management process from study start-up through database lock, including database design and data validation as per the requirements in the clinical study protocols, data review plan, & data management plan, and oversees the compliance activities across multiple CROs as...

FSP-Senior Statistical Programmer How you will contribute: • Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs) • Production and QC / validation programming • Generating complex ad-hoc reports...

Principal Medical Writer Contract, Remote Job Responsibilities • Mentors and leads less experienced medical writers on complex projects, as necessary. • Represents the Medical Writing department on clinical study teams, at conferences, meetings, and for presentations to the client regarding a writing project. • Advises clients and study teams on data presentation and production strategies and...

Senior Clinical Study Associate SUMMARY OF RESPONSIBILITIES: The Senior Clinical Study Associate (Sr. CSA) focuses on the execution of the day-to-day operational tasks associated with trial planning and conduct and is accountable as assigned by the Clinical Study Manager (CSM) or Senior CSM (Sr. CSM). This includes specific functional activities relating to the trial(s), sites, vendors, or other...