Clinical Study Manager
NAMSA · United States · US
Clinical Research
Remote
physician
Demand78
Career growth75
Healthcare fit82
Remote potential65
Salary band
USD 84k – 163k
5-year outlook
Target compensation is $115,000; with experience, CSMs can progress to Senior CSM, Clinical Project Manager, or Program Manager roles, with salary growth tied to trial complexity, device/therapeutic area, and leadership scope.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-07
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- 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
Strong option for clinicians with clinical trial or research coordination experience who want to move into CRO/MedTech study management; less suitable for those without GCP or site-facing research exposure.
Who should apply
Physicians, nurses, pharmacists, and allied health professionals with prior clinical research coordinator, site monitor, or trial site experience; IMGs seeking non-clinical CRO roles may also fit if they have GCP and regulatory exposure.
CV angle
Reframe clinical experience around trial site operations: patient screening and enrollment, informed consent, protocol adherence, adverse event reporting, regulatory documentation, IRB submissions, data quality, and cross-functional communication. Quantify study volumes, site counts, and compliance metrics where possible.
Skills to highlight
- Clinical study management
- GCP compliance
- Protocol development and training
- Site initiation and monitoring
- IRB/IEC/REB submissions
- Regulatory document collection
- Project management and tracking
- Stakeholder communication
Role summary
Clinical Study Manager at NAMSA responsible for end-to-end execution of MedTech clinical studies, including protocol materials, site start-up through close-out, regulatory submissions, site training, monitoring oversight, data quality, and client communication.
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