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Remote Clinical Data Entry Jobs in California (NOW HIRING)

RDI

Clinical Monitoring Standards Lead

Los Angeles, CA · On-site +1

... data-entry team members. The ideal candidate already knows what that means and has likely built or ... Remote candidates will be considered only if they have a proven method for learning our business ...

Tempus

Data Architect, Next Platform

Redwood City, CA · On-site +1

$150K - $200K/yr

Educate engineering and clinical teams on data modeling standards, governance, and best practices ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Initio Capital

Data Strategy Associate

San Francisco, CA · Remote

$18.75 - $24.50/hr

The Role This is a remote, flexible role for candidates who want hands-on exposure to real business problems. You may support market research, sourcing, analysis, outreach, business operations ...

Travere

Director, Clinical Science

San Diego, CA · On-site +1

$84K - $115K/yr

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Leadership position for writing clinical and data analysis reports, slide presentations ...

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All JobsClinical Data Entry JobsRemote Clinical Data Entry JobsRemote Clinical Data Entry Jobs in California

Remote Clinical Data Entry information

See California salary details

$13

$38

$85

How much do remote clinical data entry jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for remote clinical data entry in California is $38.44, according to ZipRecruiter salary data. Most workers in this role earn between $28.94 and $38.41 per hour, depending on experience, location, and employer.

Are any remote clinical data entry jobs legit?

Remote clinical data entry jobs are legitimate positions that involve inputting and managing clinical trial data from home, often requiring attention to detail and familiarity with data management software. However, job seekers should verify the employer's credibility and be cautious of scams that request upfront payments or personal information. Conducting research on the company and reading reviews can help ensure the job's legitimacy.

What does a typical workday look like for remote clinical data entry?

A typical workday in a remote clinical data entry position involves reviewing clinical documents and inputting critical data into electronic databases or health record systems. You will regularly communicate with healthcare professionals, study coordinators, or data managers to clarify details and ensure data accuracy. Most days require a balance between independent data entry tasks and virtual team meetings or status updates, all within strict privacy and compliance guidelines. The remote environment offers flexibility, but it also requires excellent self-management to meet deadlines and maintain high accuracy standards. Over time, this experience can open doors to roles in clinical data management, trial coordination, or health information analysis.

What is clinical data entry?

Clinical data entry involves inputting and managing patient information, research data, or medical records into electronic databases or systems. It requires attention to detail, accuracy, and familiarity with healthcare terminology and data management tools. This role supports clinical trials, healthcare providers, and research organizations in maintaining precise and organized medical data.

What is a remote clinical data entry?

A Remote Clinical Data Entry job involves inputting, managing, and updating clinical data in digital systems from a remote location. Professionals in this role ensure accuracy, confidentiality, and compliance with healthcare regulations. They may work with clinical trial data, patient records, or other medical information. Strong attention to detail, familiarity with medical terminology, and proficiency in data entry software are essential for success in this field.

What are the key skills and qualifications needed for remote clinical data entry?

To excel in Remote Clinical Data Entry, you need strong attention to detail, fast and accurate typing skills, and a familiarity with medical terminology, often supported by a diploma or coursework in health sciences or medical administration. Knowledge of clinical data management systems (such as EDC platforms), electronic health records (EHRs), and basic proficiency with spreadsheet software like Excel is typically required, and certification in data entry or health information management can be advantageous. Exceptional organizational skills, reliability, and the ability to work independently while maintaining clear communication with remote teams are standout soft skills for this role. These abilities ensure accurate, timely data handling, facilitate compliance with healthcare regulations, and contribute to the integrity of patient records and research data.

What are the most commonly searched types of Clinical Data Entry jobs in California?

The most popular types of Clinical Data Entry jobs in California are:

What are popular job titles related to Remote Clinical Data Entry jobs in California?

For Remote Clinical Data Entry jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Data Entry jobs in California look for?

The top searched job categories for Remote Clinical Data Entry jobs in California are:

What cities in California are hiring for Remote Clinical Data Entry jobs?

Cities in California with the most Remote Clinical Data Entry job openings:

Remote Clinical Data Entry jobs near you
Infographic showing various Remote Clinical Data Entry job openings in California as of August 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 100% Remote job distribution, with an average salary of $79,959 per year, or $38.4 per hour.

Sr. Clinical Research Associate (Field)

Shifamed

Los Gatos, CA • Remote

$120K - $140K/yr

Full-time

Re-posted 10 days ago

Job description

Supira Medical, a clinical-stage Shifamed Portfolio Company, is developing a low-profile, high continuous flow percutaneous ventricular assist device (pVAD) to provide temporary mechanical circulatory support in high risk percutaneous coronary interventional (HRPCI) procedures as well as patients suffering from cardiogenic shock. To learn more about Supira Medical, please visit www.supiramedical.com.
ABOUT SHIFAMED
Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.
Description:

We are seeking one field-based Senior Clinical Research Associate (Senior CRA) who will play a critical role in monitoring and managing clinical trial site activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. This is a full time, remote position with anticipated travel of up to 80%.

Preferred geographic locations: GA, NC, SC, TN, or TX

Responsibilities, Skills amp; Hands-On Experience:
  • Serve as the primary point of contact for investigative sites, fostering strong and collaborative site relationships.
  • Monitor patient data and clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Lead and conduct on-site and remote monitoring visits (site qualification, initiation, monitoring, and close-out) to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Critically review clinical data to ensure accuracy, completeness, and integrity in alignment with EDC systems and clinical data management standards.
  • Engage site staff in development of enrollment targets, tracking enrollment progress, and troubleshooting patient recruitment issues.
  • Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Maintain oversight of investigational product accountability, tracking, and reconciliation for cardiovascular devices.
  • Partner closely with internal stakeholders to align clinical activities with business and regulatory objectives.
  • Identify, document, and assist in resolving protocol deviations and CAPAs.
  • Participate in internal audits and support readiness for regulatory inspections.
Education amp; Work Experience:
  • Bachelor’s degree in life sciences, nursing, biomedical engineering, or related discipline.
  • 5+ years of experience in clinical research, including at least 3 years of independent monitoring for medical device trials. Experience in IDE studies strongly preferred.
  • Prior experience in cardiovascular or interventional device studies strongly preferred.
  • Strong working knowledge of GCP, ISO 14155 and FDA guidelines.
  • Proficient in EDC, eTMF, and Microsoft Office tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications. The base salary range for this full-time position is between $120,000 - $140,000 + equity + benefits.
NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.

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