Employer Active
Job Alert
You will be updated with latest job alerts via emailJob Alert
You will be updated with latest job alerts via emailBuild maintain and assure validity of metadata contained in a research data management system.
Construct metadata definitions and data fields. Program variable sequences rules and dependencies.
Review clinical protocol design system specifications metadata definitions and database infrastructure.
Works independently and closely with clients and study team to develop data transfer specification and facilitate the creation of data transfer files; Supports complex client operational service needs.
Monitor and resolve system errors.
Write and update Standard Operating Procedures and Working Instructions.
Responsible for overall performance and operation of metadata and electronic collection methodology for assigned studies.
Perform appropriate operational duties.
Actively involved in Research quality and continuous improvement initiatives. Support compliance initiatives and regulatory requirements (HIPAA ICH GCP JCAHO and others).
Bachelors degree two years clinical research experience protocol development project analyst and/or IS experience. Requires an aptitude for learning technology and applying technical skills. Candidates must possess strong project management organizational and systems thinking skills demonstrated decision-making ability and strong interpersonal and teaming skills. Attention to detail and timelines is mandatory. Successful candidates will function in a multi-task dynamic demanding work environment.
In addition individuals with experience in the following are preferred:
Visa sponsorship is not available for this position. Must be U.S. citizen permanent resident refugee or asylee. This position is not eligible for F-1 OPT STEM extension.
Required Experience:
Unclear Seniority
Full-Time