Senior Clinical Research Associate - Cardiovascular (Bilingual-English/Spanish)
MSD · United States · US
Clinical Research
Remote
Dentist
Demand82
Career growth75
Healthcare fit78
Remote potential55
Salary band
USD 129k – 203k
5-year outlook
Senior CRA compensation is generally competitive within clinical research and can progress toward CRA management, clinical trial leadership, or sponsor-side operations roles. Exact pay varies by location, sponsor, therapeutic area, and experience.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-19
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
- Dentist
- Rate period
- Annual
Why this was classified this way
- contractor
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 if you already have CRA/monitoring experience or strong clinical trial site experience and are bilingual English/Spanish. It is not an entry-level route for clinicians without prior monitoring or research experience.
Who should apply
Experienced CRAs, research nurses or clinical research coordinators, pharmacists or doctors with site monitoring/clinical trial experience, and bilingual Spanish/English professionals in South Florida or willing to travel.
CV angle
Frame real clinical trial site experience around ICH-GCP compliance, monitoring visits, regulatory documentation, CTMS/eTMF use, site relationship management, issue escalation, audit/inspection support, and bilingual communication. Quantify sites, studies, therapeutic areas, and compliance outcomes where possible.
Skills to highlight
- ICH-GCP compliance
- Site monitoring and oversight
- Clinical trial site management
- Regulatory documentation
- CTMS and eTMF systems
- Audit/inspection readiness
- Bilingual Spanish/English communication
- Cardiovascular clinical research
Role summary
A senior sponsor-side CRA role responsible for managing clinical trial sites, monitoring compliance and data quality, building site relationships, supporting audits/inspections, and mentoring junior CRAs for cardiovascular studies.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.