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Lead – Clinical Data Management - Medtech
Johnson & Johnson
$105,000 - $169,050
Aug 28, 2025
Boston, MA, USA • Bridgewater Township, NJ, USA • Washington, DC, USA • Stamford, CT, USA • Providence, RI, USA • Agawam, MA, USA • Philadelphia, PA, USA • Richmond, VA, USA • Newark, NJ, USA • Bangor, ME, USA • Concord, NH, USA • Trenton, NJ, USA • Pittsburgh, PA, USA • Burlington, VT, USA • Albany, NY, USA • Edison, NJ, USA • Norfolk, VA, USA • Bridgewater, MA, USA • Hartford, CT, USA • Syracuse, NY, USA • New York, NY, USA • Portland, ME, USA • Wilmington, DE, USA • New Haven, CT, USA • Dover, DE, USA • Baltimore, MD, USA
Johnson & Johnson is seeking a Lead, Clinical Data Management to ensure the integrity and quality of clinical trial data for their MedTech Business, while meeting project timelines and budgets.
Requirements
Experience with Electronic Data Capture (EDC), Mediciência RAVE required.
Familiarity with at least one programming language such as SAS, or R highly preferred.
Knowledge of GCP and regulatory requirements regarding clinical data management documentation and software.
Knowledge of medical terminology and use of coding dictionaries (MedDRA, WHO Drug).
Proficient in computer technology used in an office environment (Microsoft Word, Excel, etc).
Responsibilities
Independently lead several complex trials.
Lead CRF design, review and validation of clinical database, including management of CRO activities in this area as assigned if required.
Be responsible for creation of data management plans and other data management documentation as needed.
Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines partnering as appropriate with Clinical Operations, Franchise and other BSDM (Biostatistics, Statistical Programming & Data Management) functions.
Lead, coordinate, facilitate and manage all data management activities from initiation of protocol through database lock, partnering as appropriate with Clinical Operations, Franchise and other BSDM functions for their respective projects.
Proactively organize and manages ongoing data review throughout study conduct, including being responsible for the correction of errors and discrepancies management for the life of a project.
Be responsible for identification of data handling processes for non-CRF data, including lab data and image handling.
Other
Minimum of a Bachelor’s degree (or equivalent) in biological sciences, Computer Science or related discipline required; Advanced Degree strongly preferred.
At least 6+ years of clinical data management experience in Medical Device or Pharmaceuticals including experience of successful active participation in cross-functional teams required. (4+ with Advanced Degree).
Excellent verbal and written communication skills.
Mentor, train and supervise junior associates as needed in clinical data management processes and procedures.
Know and follow all laws and policies that apply to the job, and maintain the highest levels of professionalism, ethics and compliance at all times.
