Sr Clinical Research Associate

Scientific Search; San Francisco (CA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Competitive Salary and Bonus

Amazing Benefits

Opportunity for growth

Job summary

A leading clinical research organization is looking for a Senior Clinical Research Associate to oversee site management for U.S.-based clinical trials. In this remote role, you will collaborate closely with sponsors and internal teams, ensuring data integrity and compliance through all trial phases. The ideal candidate will have a relevant bachelor's degree and strong knowledge of regulatory requirements. This position includes the opportunity for meaningful travel and offers a competitive salary with additional benefits.

Qualifications

• Bachelor's degree, preferably in life sciences.
• Strong knowledge of U.S. regulatory requirements and ICH-GCP.
• Proficient with EDC, CTMS, and Microsoft Office tools.
• Highly organized with exceptional communication skills.
• Comfortable working independently in a remote, fast-paced environment.

Responsibilities

• Oversee site feasibility, selection, initiation, monitoring, and close-out activities.
• Ensure data quality through source data verification and site compliance.
• Partner with vendors, investigators, and project teams to resolve issues.
• Track enrollment, protocol deviations, and monitoring metrics.
• Support study planning, training, and electronic system development.

Skills

Strong knowledge of U.S. regulatory requirements

Exceptional communication skills

Highly organized

Proficient with EDC, CTMS, and Microsoft Office tools

Education

Bachelor’s degree in life sciences

Job description

Senior Clinical Research Associate

Location: West Coast US, Remote

Step into a pivotal role where your expertise directly shapes the success of clinical trials across multiple studies. This opportunity puts you at the center of site oversight, data integrity, and cross-functional collaboration—driving research forward where it matters most. As the senior point of contact in your region, your work will influence trial quality, timelines, and patient outcomes.

Why You Should Apply

• Make a measurable impact on the execution and oversight of U.S.-based clinical trials
• Operate with autonomy as the lead CRA across multiple investigative sites
• Collaborate with sponsors, vendors, and internal leaders on high-visibility studies
• Remote-based role with regional focus and meaningful travel
• Competitive Salary and Bonus
• Amazing Benefits and tons of opportunity for growth

What You’ll Be Doing

• Oversee site feasibility, selection, initiation, monitoring, and close-out activities
• Ensure data quality through source data verification and site compliance
• Partner with vendors, investigators, and project teams to resolve issues
• Track enrollment, protocol deviations, and monitoring metrics
• Support study planning, training, and electronic system development

About You

• Bachelor’s degree, preferably in life sciences
• Strong knowledge of U.S. regulatory requirements and ICH-GCP
• Proficient with EDC, CTMS, and Microsoft Office tools
• Highly organized with exceptional communication skills
• Comfortable working independently in a remote, fast-paced environment