Sr Clinical Research Associate

Scientific Search

🏠 Remote
📍San Francisco, CA
Posted May 20, 2026

Job Overview

Position

Sr Clinical Research Associate

Company

Scientific Search

Location

San Francisco, CA

Work Type

Remote

Job ID

li-4398294026

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

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to
[email protected]
and tell me why you’re interested. Or, feel free to email your resume. Please include
Job#19721
.

Interview Prep

AI-powered insights to help you prepare

Key Skills

Required:
Preferred:

Practice Questions

💡Technical Questions (3)
  • 1.Can you walk me through your approach to conducting source data verification at an investigative site to ensure data integrity and protocol compliance?
  • 2.How do you apply U.S. regulatory requirements and ICH-GCP guidelines when overseeing site feasibility, selection, and initiation activities?
  • 3.Describe your proficiency with EDC and CTMS systems. How do you leverage these tools to track enrollment, protocol deviations, and monitoring metrics across multiple sites?
🎯Behavioral Questions (3)
  • 1.Tell me about a time you had to resolve a significant issue at an investigative site by partnering with vendors, investigators, and internal project teams.
  • 2.Describe a situation where you had to oversee multiple clinical sites autonomously in a remote, fast-paced environment. How did you stay organized and ensure no site was neglected?
  • 3.Give me an example of a time you identified a compliance issue during a routine monitoring visit and how you handled the site close-out or corrective process.
🧩Situational Questions (2)
  • 1.You notice a significant drop in patient enrollment across your West Coast region, and one of your top investigators is unresponsive to your emails and calls. How do you handle this?
  • 2.During a site initiation visit, the site staff are highly resistant to adopting the study's electronic systems, claiming they are too complex and disrupt their workflow. How do you ensure successful system adoption?

Resume Keywords

Make sure these keywords appear on your resume

Site MonitoringSource Data VerificationICH-GCPEDCCTMSProtocol DeviationsSite InitiationEnrollment TrackingRegulatory ComplianceCross-functional CollaborationData IntegrityClinical Trials

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