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Scalence

Optometric Assistant

Pay: $57,200/yr

Posted: 8 weeks ago

Location: San Jose, CA (Onsite)

Last Updated: 3 weeks ago

Hours: Full-Time

Expires: 9/12/2026

Career Insights for Clinical Data Analyst

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What they do

A Clinical Data Analyst is responsible for gathering, compiling, modeling, validating, and analyzing clinical trial results data needed by pharmaceutical companies, governmental agencies, and biotechnology firms evaluate the effectiveness of their trial drugs. May be responsible for designing, testing, and implementing clinical data reporting systems for the clinical staff to use.

$83,653 / year median in California

-7% projected decline

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Job Description

Job Overview 1. Rx Lens Order Management & Input Accurately input complex prescription lens data into ordering systems. Verify lens parameters Communicate with optical labs to troubleshoot order delays or specification discrepancies. Verify incoming lenses 2. Tracking & Inventory Control Maintain a real-time tracking log of all pending, shipped, and received lens orders.

Device accountability:

Manage physical and digital inventory of frames and lenses Conduct regular audits to ensure inventory levels align with study recruitment targets. 3. Clinical Documentation & Assistant Support Support the Lead Coordinator in maintaining the Trial Master File (TMF) and site-specific regulatory binders. Assist in the preparation and filing of IRB (Institutional Review Board) submissions, amendments, and continuing reviews. Data entry, data collection, and query resolution Ensure all participant "Source Documentation " is accurate, legible, and compliant with ALCOA+ principles. 4. Regulatory Compliance Facilitate the Informed Consent process for study participants, ensuring all ethical and regulatory requirements are met. Adhere strictly to GCP (Good Clinical Practice) and HIPAA guidelines regarding participant privacy and data integrity.

Required Qualifications Experience:

Minimum of 1 year of experience in clinical research or similar regulatory role.

Regulatory Knowledge:

Proven experience working with IRBs, managing the consenting process, and maintaining clinical study documentation.

Technical Accuracy:

High level of comfort with data entry where precision is critical (familiarity with ophthalmic prescriptions is a plus).

Organization:

Exceptional tracking skills; ability to manage high volumes of hardware/inventory without loss of data integrity.

Communication:

Strong professional presence for participant interaction and clear technical communication with lab partners. GCP certification Preferred Skills Familiarity with optical and ophthalmic terminology Previous experience in a device-based clinical trial environment

Pay:

$25.00 - $30.00 per hour

Work Location:

In person