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Electronic Data Capture Jobs (NOW HIRING)

We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...

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We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...

Accurately document study data in electronic data capture systems and patient records. * Maintain regulatory binders and essential documents. * Ensure data integrity and confidentiality.

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Collaborate with data management staff to support data entry into electronic data capture (EDC) systems and assist with query resolution. * Work with regulatory staff to support compliance activities ...

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Collaborate with data management staff to support data entry into electronic data capture (EDC) systems and assist with query resolution. * Work with regulatory staff to support compliance activities ...

Apply Early

... capture efforts. · Services may be required to be provided at supplier's site using supplier's equipment. · Typically need an end product of electronic data, typically transmitted through FTP. · ...

Collect, manage, and accurately enter clinical study data into electronic data capture (EDC) systems. * Conduct data quality checks, identify discrepancies, and collaborate with study teams to ...

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Electronic Data Capture information

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How much do electronic data capture jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for electronic data capture in the United States is $28.44, according to ZipRecruiter salary data. Most workers in this role earn between $15.87 and $35.82 per hour, depending on experience, location, and employer.

What is an Electronic Data Capture job?

An Electronic Data Capture (EDC) job involves managing digital systems used to collect, store, and process clinical trial or research data. Professionals in this role ensure data accuracy, integrity, and compliance with regulatory standards. They may configure EDC systems, troubleshoot technical issues, and support researchers or study personnel in data entry and validation. Strong analytical, technical, and problem-solving skills are essential in this position.

What are the key skills and qualifications needed to thrive in the Electronic Data Capture position, and why are they important?

To thrive in Electronic Data Capture, you need a solid understanding of clinical data management, data entry accuracy, and regulatory compliance, often supported by a degree in life sciences or information technology. Familiarity with EDC systems such as Medidata Rave or Oracle InForm, as well as certifications like Certified Clinical Data Manager (CCDM), are commonly required. Attention to detail, strong organizational skills, and effective communication are valuable soft skills in this field. These competencies are important for ensuring the integrity, security, and efficiency of electronic clinical trial data collection and management.

What are typical daily responsibilities for someone working in Electronic Data Capture?

Professionals in Electronic Data Capture are responsible for designing and managing electronic case report forms (eCRFs), monitoring data entry for accuracy and completeness, and ensuring compliance with clinical trial protocols and regulatory standards. Daily tasks may also include troubleshooting EDC system issues, coordinating with clinical research teams, and preparing data reports for study progress reviews. Collaboration with data managers, IT specialists, and regulatory staff is common, so teamwork and clear communication are essential. Staying organized and detail-oriented helps ensure the integrity and quality of collected data, which is critical for the success of clinical research projects.

Is data capturing a difficult job?

Electronic Data Capture (EDC) jobs involve collecting, managing, and ensuring the accuracy of data, often requiring attention to detail and familiarity with data management tools. The difficulty depends on the complexity of the data, the tools used, and the experience of the individual, but it generally requires strong organizational skills and adherence to protocols.

What qualifications do I need to be a data capturer?

A data capturer typically needs a high school diploma or equivalent, strong attention to detail, and proficiency with data entry tools such as spreadsheets or database software. Good organizational skills and the ability to work efficiently under deadlines are also important; some roles may require familiarity with specific data management systems or basic knowledge of data privacy standards.

How can I make 2000 a week working from home?

Electronic Data Capture (EDC) professionals can earn around $2,000 weekly by working as freelance or contract data entry specialists, clinical data managers, or remote EDC analysts, often requiring skills in database management, attention to detail, and familiarity with EDC software. Achieving this income typically involves working full-time hours, gaining relevant certifications, and building experience in the healthcare or research industries. Remote EDC roles may also involve flexible schedules and the use of tools like electronic data capture platforms and project management software.

What is the highest paying data entry job?

The highest paying data entry jobs typically involve specialized roles such as medical or legal transcriptionists, data analysts, or roles requiring advanced skills in database management and software tools. These positions often offer higher salaries due to increased expertise, certifications, and experience, with some earning over $50,000 annually depending on the industry and location.
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Research (LPN) In-person

Smith Allergy and Asthma

Horseheads, NY • On-site

$28 - $32/hr

Full-time

Posted 29 days ago

Be an early applicant


Job description

About the Role:

The Research (LPN) plays a pivotal role in managing and overseeing clinical trials to ensure they are conducted in compliance with regulatory standards and study protocols. This position involves coordinating patient recruitment, data collection, and communication between study participants and the research team to facilitate smooth trial operations. The coordinator ensures accurate documentation and reporting of clinical data, maintaining the integrity and confidentiality of patient information. By collaborating closely with investigators, sponsors, and regulatory bodies, the coordinator helps advance medical research and contributes to the development of new treatments. Ultimately, this role supports the successful execution of clinical studies that improve patient outcomes and advance healthcare knowledge.

Minimum Qualifications:

  • Licensed Practical Nurse (LPN) credential in the United States.
  • Basic knowledge of clinical research principles and regulatory requirements.
  • Experience in patient care and clinical procedures.
  • Strong organizational and communication skills.
  • Ability to work collaboratively in a multidisciplinary team environment.

Preferred Qualifications:

  • Previous experience as a Clinical Research Coordinator or in clinical trial settings.
  • Certification in Clinical Research (e.g., CCRC or equivalent).
  • Familiarity with electronic data capture (EDC) systems and clinical trial management software.
  • Knowledge of FDA regulations and Institutional Review Board (IRB) processes.
  • Experience with patient recruitment and retention strategies.

Responsibilities:

  • Coordinate and manage daily clinical trial activities including patient screening, enrollment, and follow-up visits.
  • Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
  • Collect, record, and maintain accurate clinical data and patient records in electronic data capture systems.
  • Serve as the primary liaison between patients, investigators, and sponsors to facilitate communication and resolve issues.
  • Monitor patient safety and report adverse events promptly according to protocol and regulatory guidelines.
  • Schedule and conduct study visits, including obtaining informed consent and performing clinical assessments.
  • Assist in the preparation and submission of regulatory documents and study reports.
  • Maintain inventory of study supplies and ensure proper storage of investigational products.

Skills:

The Clinical Research Coordinator (LPN) utilizes clinical nursing skills daily to perform patient assessments, administer treatments, and monitor patient safety during trials. Strong organizational skills are essential for managing multiple study protocols, scheduling visits, and maintaining accurate documentation. Effective communication skills facilitate clear interactions with patients, investigators, and sponsors, ensuring all parties are informed and engaged. Knowledge of regulatory guidelines and clinical research processes ensures compliance and ethical conduct throughout the study lifecycle. Additionally, proficiency with electronic data systems supports accurate data entry and reporting, which is critical for the integrity and success of clinical trials.