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Edc Jobs in California (NOW HIRING)

Actalent

Clinical Research Coordinator

Redwood City, CA

$30 - $45/hr

Proficiency with electronic data capture (EDC) systems for clinical research. * Experience with electronic medical records (EMR) and chart review in a clinical setting. * Proven experience in patient ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT), including contribution to system requirements and validation activities * Oversee vendor performance ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT), including contribution to system requirements and validation activities * Oversee vendor performance ...

Collabera

Clinical Data Manager

Irvine, CA

Perform data management activities on both Electronic Data Capture (EDC) and paper studies. Major activities include Performs as lead data manager for projects and/or programs Responsible for the ...

AbbVie

System Design Analyst II - HYBRID

Irvine, CA · On-site

Veeva EDC technical study build experience is a plus. * In-depth knowledge of clinical trial processes. * In-depth knowledge of CDASH (Required) and SDTM. * Demonstrated performance as a key ...

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How much do edc jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for edc in California is $24.81, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $28.46 per hour, depending on experience, location, and employer.

What are some common challenges faced by EDC professionals in clinical research, and how can they be managed?

Professionals working with Electronic Data Capture (EDC) systems in clinical research often encounter challenges such as ensuring data accuracy, maintaining regulatory compliance, and managing system updates. These challenges can be managed by staying up-to-date with industry regulations, participating in ongoing training, and collaborating closely with clinical teams to streamline data entry processes. Regular communication with IT and data management teams is also crucial to address technical issues promptly and ensure smooth workflows.

What are the key skills and qualifications needed to thrive as an EDC specialist?

To thrive as an EDC Specialist, you need a solid understanding of clinical data management, data integrity principles, and experience with electronic data capture in clinical trials, often supported by a degree in life sciences or related fields. Familiarity with EDC systems like Medidata Rave or Oracle InForm, and certifications such as CDISC or GCP, are typically required. Attention to detail, problem-solving, and strong communication skills help you effectively collaborate with clinical teams and ensure high-quality data collection. These skills are crucial for accurate, compliant data management, which underpins the success of clinical research projects.

What is an EDC?

EDC stands for 'Everyday Carry.' In the context of jobs, an EDC typically refers to the essential tools, gadgets, or items that someone carries daily to be prepared for work or emergencies. This can include multitools, flashlights, pocket knives, pens, and other items tailored to the individual's profession or needs. People in security, law enforcement, medical fields, or even office environments often have different EDC items. The concept emphasizes practicality, preparedness, and efficiency in daily tasks.
What job categories do people searching Edc jobs in California look for? The top searched job categories for Edc jobs in California are:
What cities in California are hiring for Edc jobs? Cities in California with the most Edc job openings:
Edc jobs near you
Infographic showing various Edc job openings in California as of August 2026, with employment types broken down into 87% Full Time, 6% Part Time, 2% Temporary, and 5% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $51,596 per year, or $24.8 per hour.

Clinical Research Coordinator (CRC)

Smarter HR Solutions LLC

Orange, CA

$90K - $100K/yr

Full-time

Re-posted 10 days ago

Job description

Job description
Job Title: Clinical Research Coordinator (CRC)
Job Type: Full-Time
Job Location(s): Orange, CA *This role is ONSITE*
Job Salary: $32-$35/hour ($66,560.00 - $72,800.00 per year)
Job Schedule: M-F 40-hours/week

This is an on-site position in Orange, CA, and applicants must reside within a commutable distance of 50 miles or less or be able to independently relocate. THIS IS NOT A REMOTE POSITION.


Position Summary

The Clinical Research Coordinator will support the planning, execution, and closeout of clinical studies involving human subjects. This includes FDA-regulated drug and device trials, NIH-funded research, and investigator-initiated protocols. The CRC ensures compliance with California-specific regulatory frameworks, institutional policies, and federal guidelines (FDA, ICH-GCP, HIPAA).


Experience in CRC in Liver/GI/Obesity studies preferred!

Key Responsibilities

Study Operations

  • Coordinate Phase I–IV clinical trials across multiple therapeutic areas.
  • Prepare IRB submissions, amendments, and continuing reviews.
  • Develop and maintain study documentation, SOPs, and case report forms.
  • Schedule and conduct study visits, collect data, and ensure protocol adherence.

Participant Management

  • Recruit, screen, and consent participants in accordance with CPHS and institutional HRPP standards
  • Educate participants on study procedures, risks, and rights
  • Monitor for adverse events and report per FDA and California Health & Safety Code §24170–24179.5

Regulatory & Compliance

  • Maintain audit-ready records and ensure GCP compliance
  • Handle protected health information (PHI) securely under California law
  • Liaise with sponsors, monitors, and regulatory bodies

Data & Budget Oversight

  • Enter and validate data in CTMS and EDC systems
  • Assist with budget development and financial tracking
  • Coordinate biospecimen collection, processing, and shipping

Job Type: Full-time

Work Location: In person



Requirements
Qualifications

Education

  • Bachelor’s degree in health sciences, biology, nursing, or related field (Master’s preferred).
  • Formal training in clinical research or regulatory affairs.


Experience
  • 1–3 years of clinical research coordination experience, primarily in liver/GI/obesity studies.
  • Familiarity with California IRB systems and CPHS protocols.
  • Experience with FDA-regulated trials and NIH-funded studies.


Skills
  • Strong organizational and time management abilities.
  • Excellent verbal and written communication skills.
  • Proficiency in CTMS, EDC, and IRB platforms (e.g., iRIS, OnCore).
  • Ability to work independently and collaboratively across teams
  • Preferably bilingual in English/Spanish