Senior Clinical Research Specialist
Becton Dickinson · Irvine Laguna Canyon, CA
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Becton Dickinson seeks a Senior Clinical Research Specialist to lead the planning, execution, and oversight of clinical research studies for medical devices. The role ensures regulatory compliance, manages trial operations from initiation to close-out, and collaborates with cross-functional teams to support product development and market approval.
What they're looking for
- Bachelor's degree in scientific, biomedical engineering, or health-related field; Master's preferred
- Minimum 5 years clinical research experience, preferably in medical device industry
- Knowledge of Good Clinical Practice (GCP), FDA regulations, and ISO 14155 standards
- Proven experience managing clinical trials from initiation through close-out
- Understanding of trial design, data collection, and statistical principles
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC)
- Domestic and international travel up to 20% as needed
What you'll be doing
- Lead design, development, and review of clinical study protocols and informed consent forms
- Manage day-to-day trial operations including site selection, initiation, monitoring, and close-out
- Ensure GCP and regulatory compliance across all assigned clinical studies
- Conduct data review, query resolution, and contribute to analysis of trial data
- Present study updates and findings to internal and external stakeholders
Privacy & handoff
This role links to Becton Dickinson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.