Research Science Management
Intuitive · United States · US
Clinical Research
Remote
physician
Demand72
Career growth68
Healthcare fit82
Remote potential45
5-year outlook
Likely a solid mid-career clinical research/medtech program management pathway with compensation above many academic research roles, but exact salary will depend on location, seniority, and prior industry experience. Growth into senior program leadership, clinical affairs, or evidence strategy is plausible.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-11-06
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- License jurisdiction
- US
- Profession fit
- physician
- Rate period
- Annual
Why this was classified this way
- Contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for clinicians who already have clinical research, clinical affairs, or research program management experience and want a medtech digital-health evidence role. It is less suitable for clinicians without prior study management or industry research exposure because the experience barrier is substantial.
Who should apply
Physician-scientists, research nurses, pharmacists with outcomes research or clinical trials experience, allied health professionals with study coordination/management backgrounds, and IMGs with clinical research or CRO/medtech experience.
CV angle
Frame real clinical and research experience around study design, protocol and consent development, IRB/EC submissions, GCP/CFR compliance, budget and timeline management, CRO/vendor oversight, publication support, and stakeholder relationships with investigators, OR staff, and health-system leaders. Emphasize measurable project delivery and evidence-generation outcomes without overstating industry experience.
Skills to highlight
- Clinical research study management
- IRB and Ethics Committee submissions
- GCP and CFR compliance
- Protocol and informed consent development
- Budget and timeline management
- CRO/vendor management
- Publication development and peer-review response
- Stakeholder and KOL relationship management
Role summary
A Scientific Research Program Manager role at Intuitive managing internal and collaborative evidence-generation studies for digital products and services, including study start-up, budgets, investigator selection, IRB/EC submissions, CRO oversight, compliance, publications, and stakeholder communication.
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