Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

OfficeJoin Us as a Senior Clinical Data Associate Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years As part of our expert team youll have the opportunity to ensure operational excellence that makes a real difference in organizational performance As a Senior Clinical Data Associate you will perform all aspects of the data cleaning process with minimal supervision in accordance with Good Clinical Practices GCP and Standard Operating ProceduresWork Process Documents SOPsWPDs to assess the safety and efficacy of investigational products andor medical devices What Youll Do Supports the setup of study activities such as database design testing of data entry screens and Data Validation Manual DVM creation as required Reviews data listings for accuracy and consistency of data Acts as point person and subject matter expert for specialized studyspecific processes Generates tracks and resolves data clarifications and queries and makes changes to the clinical database as required Contributes to the improvement of data management processes on a global level Produces projectspecific status reports for management andor clients on a regular basis Provides training and work direction to junior staff as required Education and Experience Requirements Bachelors degree or equivalent and relevant formal academic vocational qualification Previous experience that provides the knowledge skills and abilities to perform the job comparable to 0 to 2 years In some cases an equivalency consisting of a combination of appropriate education training andor directly related experience will be considered sufficient for an individual to meet the requirements of the role Knowledge Skills and Abilities Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines global SOPs and client expectations Strong attention to detail and skill with numbers Good written and verbal communication skills Good analyticalproblemsolving skills Ability to maintain a high degree of confidentiality with clinical data and clients proprietary data Strong customer focus and excellent interpersonal skills Proven flexibility and adaptability Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands Knowledge of medicalclinical terminology Understands project protocol and DVM Proven ability in achieving applicable technical competencies per the DM competency grid Working Conditions and Environment Work is performed in an office environment with exposure to electrical office equipment Occasional drives to site locations Occasional travel both domestic and international Why Join Us When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference Apply today to help us deliver tomorrows breakthroughs