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Principal Scientist, Clinical Research – MedTech Surgery
Job in
California, Moniteau County, Missouri, 65018, USA
Listed on 2026-08-25
Listing for:
Jobtailor
Full Time
position Listed on 2026-08-25
Job specializations:
-
Healthcare
Clinical Research, Medical Science
Job Description & How to Apply Below
- Provide scientific leadership for Johnson & Johnson Med Tech Surgery's Robotic Surgery Platform
- Collaborate with multi-functional evidence teams, including Medical, Clinical, Pre-clinical, and Health Economics and Market Access
- Develop and deliver global evidence generation strategies for pre- and post-market approval studies, investigator-initiated studies, and real-world evidence
- Ensure input and alignment from strategically important regional Med Tech leads
- Design clinical trials to meet premarket and post-market needs
- Strengthen capability in and drive implementation of real-world evidence
- Develop a network with key surgeons in the US, EU, and APAC to assist in execution of Robotic Surgery clinical trials
- Lead cross-functional teams to interpret and disseminate evidence, including CSRs, abstracts, and manuscripts
- Support clinical scientific discussions with regulatory agencies and notified bodies
- Review clinical evidence generated for marketing authorization and line extensions, including during sponsor regulatory inspections
- Provide scientific, technical, and strategic assessment of new business development opportunities and support acquisition of innovative products
- Influence, shape, and lead teams
- Build relationships internally and partnerships with business partners and customers/investigators
- Travel domestically up to 25% as required
- A minimum of a Bachelor’s degree in Biological Science, Engineering, or a related field is required
- A minimum of 8 years of related scientific / technical experience within Clinical Research required
- Expertise in clinical research science and processes
- Broad and extensive understanding of product development processes, team dynamics, healthcare market environment, clinical trends, and global clinical trial regulations
- Proven track record of contributing to clinical programs within a clinical or surgical research setting, on time, within budget, and in compliance with SOPs and US regulations
- Experience working in Robotics strongly preferred
- Experience supporting global regulatory submissions for medical devices, biologics, or drugs preferred
- Up to 25% domestic travel may be required
Demonstrates expertise in clinical research science and processes, with a strong focus on developing and delivering evidence generation strategies for clinical trials. Proven ability to lead cross-functional teams and build relationships with key stakeholders in the healthcare market.
Highest-signal resume keywords- Clinical Research Science Expertise
- Robotics Experience
- Global Regulatory Submissions
- Clinical Trial Design
- Evidence Generation Strategies
- Clinical Research
- Evidence Generation
- Clinical Trial Design
- Regulatory Compliance
- Product Development Processes
- Surgical Research
- Data Interpretation
- Budget Management
- Strategic Assessment
- Real-World Evidence
- Leadership
- Collaboration
- Relationship Building
- Influencing
- Communication
- Medical Devices
- Biologics
- Clinical Trials
- Healthcare Market
- Global Clinical Trial Regulations
- SOP Compliance
- Market Access
- Health Economics
- Pre-Clinical Studies
- Post-Market Approval
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