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Senior Principal Clinical Research Specialist
Job in
California, Moniteau County, Missouri, 65018, USA
Listed on 2026-09-14
Listing for:
Jobtailor
Full Time
position Listed on 2026-09-14
Job specializations:
-
Science
Clinical Research, Medical Science
Job Description & How to Apply Below
- Lead the planning, execution, and oversight of complex clinical studies and clinical development programs supporting Neurovascular therapies
- Provide strategic leadership for one or more large clinical studies, ensuring study objectives, timelines, quality standards, and business priorities are achieved
- Manage multiple studies, work streams, and competing priorities simultaneously
- Develop and execute clinical evidence generation strategies supporting regulatory, commercial, and product development objectives
- Partner with Clinical, R&D, Regulatory Affairs, Quality, Medical Affairs, Marketing, Health Economics & Reimbursement, and other stakeholders
- Liaise with physicians, investigators, external clinical partners, and other stakeholders throughout study execution
- Present clinical study strategy, progress, risks, and outcomes to senior and executive leaders
- Author and review clinical, scientific, and regulatory documentation, including protocols, clinical study reports, publications, presentations, and submission materials
- Interpret, analyze, and communicate complex clinical data and study outcomes to technical and non-technical audiences
- Lead publication and dissemination activities with physician investigators, key opinion leaders, and internal stakeholders
- Monitor emerging scientific literature, competitive developments, and evolving clinical evidence in the neurovascular therapeutic area
- Bachelor's degree in a technical discipline and 10+ years of relevant clinical research or medical device experience, or an advanced degree with 8+ years of relevant experience
- Demonstrated experience independently leading complex clinical studies or clinical development programs
- Proven experience owning study strategy, execution, timelines, stakeholder management, and program outcomes
- Strong clinical study management expertise within a regulated healthcare, life sciences, or medical device environment
- Experience interacting with senior leadership and presenting clinical information to executive audiences
- Exceptional stakeholder management, influencing, organizational, and communication skills
- Ability to independently drive outcomes and operate effectively in a highly matrixed environment
- Doctor of Medicine (MD) or Doctor of Philosophy (PhD) in a biomedical science discipline preferred
- Neurovascular clinical research experience strongly preferred
- Experience leading global and/or multi-site clinical studies
- Experience serving as a Clinical Trial Director, Clinical Trial Lead, Senior Clinical Program Lead, or comparable leadership-level clinical research role
- Experience managing complex clinical trials involving multiple stakeholders and work streams
- Experience engaging investigators, physicians, and external clinical partners
- Demonstrated executive presentation and leadership communication skills
- Experience supporting regulatory submissions and health authority interactions
- Strategic mindset with the ability to influence decisions across functions and leadership levels
- For Baccalaureate degrees earned outside of the United States, a degree satisfying 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
- Unrestricted U.S. work authorization is required at hire and throughout employment for roles below Principal level
Demonstrates extensive expertise in leading complex clinical studies and development programs within the neurovascular therapeutic area, with a strong focus on stakeholder management, regulatory submissions, and strategic communication. Proven ability to drive outcomes in a matrixed environment while effectively presenting clinical information to executive leadership.
Highest-signal resume keywords- Clinical Study Management
- Regulatory Submissions
- Stakeholder Management
- Neurovascular Clinical Research
- Executive Presentation Skills
- Clinical Research
- Clinical Development Programs
- Data Analysis
- Protocol Development
- Clinical Study Reports
- Health Economics
- Regulatory Affairs
- Medical Device Experience
- Complex Clinical Trials
- Strategic Leadership
- Organizational Skills
- Communication Skills
- Influencing Skills
- Leadership Skills
- Collaboration Skills
- Doctor of Medicine (MD)
- Doctor of Philosophy (PhD)
- Neurovascular Therapies
- Life Sciences
- Healthcare
- Clinical Trial Director
- Multi-Site Clinical Studies
Position Requirements
10+ Years
work experience
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