Role OverviewThe EDC Clinical Trial Designer will create high-quality data collection tools for new clinical trials and facilitate activities related to the design, development, documentation, testing, and implementation of clinical eCRF databases.
What You Will Do
Design of eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio, ensure standard operating procedures and guidelines are implemented, and validate study design for forms and schedule design.
Why It Might Be a Fit
The ideal candidate will have a strong attention to detail, commitment to high-quality work, and experience in clinical data management and database design.
Requirements
- BA/BS degree
- Minimum of 2 years of Clinical Data Management experience using electronic data capture systems
- Effective oral and written presentation and communication skills
- Strong attention to detail and a commitment to high-quality work, customer service, and getting things right the first time with minimal errors
- Ability to manage multiple project tasks and deliverables in a fast-paced constantly changing environment
- Experience in the planning and management of clinical trials in the biopharmaceutical industry or a related field is preferred
- Familiarity with clinical research processes and CDISC/CDASH/SDTM standards is preferred
Benefits
- Health and welfare benefits
- Other benefits
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