Senior Clinical Research Associate (Fully Remote)

Not Disclosed; United States; Remote; USD 90,000 - 120,000; Full time

Job summary

Not Disclosed is seeking a Senior Clinical Research Associate to oversee complex clinical studies and ensure high-quality monitoring across study sites. The role emphasizes on-site leadership, data integrity, and cross-functional collaboration.

The candidate will train and mentor junior CRAs, coordinate with investigators and project teams, and contribute to audit readiness, regulatory documentation, and QA support within a dynamic CRO setting.

Qualifications

• College or university degree in Life Sciences or equivalent experience.
• At least 3 years of independent, on-site clinical monitoring experience.
• Full professional proficiency in Spanish and English.
• Tailored training courses and professional mentoring for career development.
• Opportunity to develop skills in training, mentoring, and leadership.
• Exposure to complex clinical studies and potential progression to Lead Monitor.

Responsibilities

• Prepare, conduct, and report site selection, initiation, monitoring, and closeout visits.
• Perform CRF reviews, source document verification, and clinical data query resolution.
• Support audit preparation and assist Regulatory Affairs teams with documentation.

Skills

Clinical monitoring

Mentoring

Training

Bilingual English/Spanish

Education

Life Sciences degree

Job description

• Senior Clinical Research Associate overseeing complex clinical studies.
• Responsible for training, mentoring, and coordinating junior CRAs.
• Key liaison between investigators, site staff, and project teams.

Key Responsibilities:

• Prepare, conduct, and report site selection, initiation, monitoring, and closeout visits.
• Perform CRF reviews, source document verification, and clinical data query resolution.
• Support audit preparation and assist Regulatory Affairs teams with documentation.

Requirements:

• College or university degree in Life Sciences or equivalent experience.
• At least 3 years of independent, on-site clinical monitoring experience.
• Full professional proficiency in Spanish and English.
• Tailored training courses and professional mentoring for career development.
• Opportunity to develop skills in training, mentoring, and leadership.
• Exposure to complex clinical studies and potential progression to Lead Monitor.

Not Disclosed

The partner company is a clinical research organization specializing in complex clinical studies. It fosters a people-focused culture with opportunities for professional growth and mentoring.