Senior Clinical Program Manager
Posted 2026-05-06
Remote, USA
Full-time
Immediate Start
- Job Description:
- Integrate with R&D during product development for new device indications
- Partner with Regulatory, Marketing, and R&D to design pre-market feasibility and pivotal clinical studies
- Collect clinical safety and performance data to meet regulatory requirements
- Work with key stakeholders to ensure appropriate data elements are captured during CRF development
- Assist in internal and external audits
- Requirements:
- Bachelor’s degree required
- Minimum of 5 years’ medical device clinical study experience
- Knowledge of, and experience with, the FDA and the EU regulatory environments
- Excellent written and verbal communication skills
- Strong analytical, critical thinking, and problem-solving skills
- Ability to participate in high-level technological and clinical discussions
- Proficient in Microsoft Office, Word, and Power Point
- Benefits:
- health, dental, and vision insurance
- life insurance
- short-term and long-term disability insurance
- 401(k)
- paid time off
- more