Senior Clinical Research Associate

AL Solutions; California (MO); Remote; USD 72,000 - 115,000; Full time

Job summary

A leading life science company seeks a Senior Clinical Research Associate to remotely manage and monitor clinical trials. The role requires fluency in Spanish and English, alongside 4+ years of CRA experience. Candidates will mentor others while ensuring data integrity and compliance across studies.

Qualifications

• 4+ years of CRA experience with senior-level responsibilities.
• Strong knowledge of ICH-GCP and FDA regulations.
• Broad therapeutic area exposure preferred.

Responsibilities

• Lead and execute monitoring activities across diverse sites.
• Mentor junior CRAs and contribute to onboarding.
• Ensure adherence to study protocols and regulatory standards.

Skills

Monitoring activities

Bilingual fluency in Spanish and English

Regulatory compliance

Data integrity

Job description

Direct message the job poster from AL Solutions

Connecting Clinical Operations professionals with extraordinary Life Science companies globally

Are you a seasoned CRA ready to step into a senior-level role and make a measurable impact in clinical research? We’re seeking a Senior Clinical Research Associate fluent in Spanish and English, with extensive experience across multiple clinical trial phases and therapeutic areas.

This role offers the flexibility of remote work combined with the opportunity to support high-impact studies in a collaborative, quality-driven environment.

Role Overview:

• Position: Senior Clinical Research Associate (Senior CRA)
• Location: U.S. (Remote, with regional or national travel)
• Experience: 4+ years of CRA experience, with demonstrated senior-level responsibilities

Key Responsibilities:

• Independently lead and execute monitoring activities across diverse sites and study phases (I–IV)
• Serve as the primary contact for investigative sites, ensuring adherence to study protocols and regulatory standards
• Mentor junior CRAs and contribute to onboarding and training activities
• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure data integrity, patient safety, and regulatory compliance across all assigned studies
• Collaborate cross-functionally with project management, medical, and data teams
• Minimum 4 years of experience as a CRA, with progression to senior-level tasks (e.g., site leadership, mentorship, complex protocols)
• Bilingual fluency in Spanish and English (spoken and written) is required
• Broad therapeutic area exposure preferred (e.g., oncology, CNS, cardiology, infectious diseases)
• Strong knowledge of ICH-GCP, FDA regulations, and electronic data capture systems
• Ability to travel regionally/nationally as needed

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Health Care Provider

• Industries

  Staffing and Recruiting and Pharmaceutical Manufacturing

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