Clinical Research Coordinator

How to use this kit

Ground every answer in facts on this page and the original listing. We never invent Glassdoor-style reviews or salaries that are not in our data.

Interview prep

Be ready to walk through screening, informed consent support, source documentation, and how you escalate adverse events. Expect scenario questions on eligibility conflicts and protocol deviations.

Fit summary

Strong fit if you are detail-oriented, calm with patients, and comfortable with strict documentation in an on-site La Mesa clinical research setting at ALLIANCE CLINICAL.

Day in the role

As a Clinical Research Coordinator at ALLIANCE CLINICAL in La Mesa, you would typically:

• Screen and schedule study subjects per protocol
• Run protocol procedures (interviews, vitals, ECGs)
• Prepare IRB docs, worksheets, and adverse-event reports
• Educate participants and log side effects with investigators

Skills to emphasize

Build protocol literacy, GCP-style documentation, subject communication, and AE reporting.

• Saylor Academy — Health Sciences courses (free)
• Coursera — audit-track healthcare courses (free to learn)

FAQ from this listing

Is this role remote?

No—the listing indicates on-site work in La Mesa, San Diego County.

What does a Clinical Research Coordinator do day to day?

Schedule and screen subjects, perform protocol procedures, prepare study documents, and report adverse events with investigators.

Where can I start learning for free?

Saylor Academy Health Sciences courses are free; Coursera audit-track healthcare courses are free to learn.

Occupation tasks (O*NET)

Public-domain labor data — prepare examples for 2–3 of these.

• Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
• Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
• Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
• Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• Inform patients or caregivers about study aspects and outcomes to be expected.
• Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
• Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
• Oversee subject enrollment to ensure that informed consent is properly obtained and documented.

O*NET source

Company facts (cached)

Website: allianceclinical.com

Public cache only — not an employee review.

Role overview (listing rewrite)

Clinical Research Coordinator at ALLIANCE CLINICAL in La Mesa, San Diego County Position Summary The Clinical Research Coordinator (CRC) supports the coordination and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are conducted in compliance with regulatory requirements and ethical standards. The position is full-time and temporary, currently estimated to last until December 31, 2026, but may become permanent based on business needs. Core Duties Assist in the planning, organization, and implementation of clinical research studies Ensure compliance with regulatory requirements, including IRB/IECs and FDA guidelines Coordinate with study teams to ensure timely data collection and reporting Support participant recruitment and retention efforts Maintain accurate documentation of study activities and progress Who We're Looking For We are seeking a detail-oriented and organized individual with experience in clinical research. The ideal candidate should have excellent communication skills, be able to work independently, and possess strong attention to detail. More About ALLIANCE CLINICAL ALLIANCE CLINICAL is dedicated to advancing medical knowledge through high-quality clinical trials. Our team of professionals works collaboratively to ensure that every study meets the highest standards of integrity and ethical conduct. Ready to Apply? To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.

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Questions to ask them

• What does success look like in the first 90 days for this role?
• How is the team structured, and who would I work with most?
• What tools and systems does this role use daily?
• Is the work primarily based in La Mesa, San Diego County, hybrid, or fully remote?