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Full Time Edc Programmer Jobs (NOW HIRING)

VTG

Financial Analyst

Washington, DC

$70K - $100K/yr

... Planning, Programming, Budgeting, and Execution (PPBE)). * Proficiency with Navy Financial ... UNAVAILABLEEmployment Type: FULL_TIME

The Doe Fund Inc

Maintenance Worker

Brooklyn, NY · On-site

The Doe Fund is also one of New York City's largest nonprofit developers of permanent affordable ... EDC to provide support services for its Clean-Up Corp Programs hiring approximately 55 full-time ...

Alphatec Spine

Clinical Scientist II

Carlsbad, CA

$125K - $140K/yr

Prepare clear, complete and accurate technical engineering documentation. * Contribute to the ... Familiarity with electronic data capture systems (EDC, EMR), data analysis, and data visualization.

Alphatec Spine

Clinical Scientist II

Carlsbad, CA · On-site

$125K - $140K/yr

Prepare clear, complete and accurate technical engineering documentation. * Contribute to the ... Familiarity with electronic data capture systems (EDC, EMR), data analysis, and data visualization.

Alphatec Spine

Clinical Scientist II

Carlsbad, CA · On-site

$125K - $140K/yr

Prepare clear, complete and accurate technical engineering documentation. * Contribute to the ... Familiarity with electronic data capture systems (EDC, EMR), data analysis, and data visualization.

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

This position requires a full-time onsite presence at our Redmond, WA office. Responsibilities ... Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial ...

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How much do full time edc programmer jobs pay per hour?

As of May 30, 2026, the average hourly pay for full time edc programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time EDC Programmer, and why are they important?

To thrive as a Full Time EDC Programmer, you need strong programming skills (often in languages like SQL, Python, or SAS), a solid understanding of clinical data management, and typically a degree in computer science or a related field. Familiarity with Electronic Data Capture (EDC) systems such as Medidata Rave or Oracle InForm, and certifications in clinical data management or EDC platforms, are highly beneficial. Attention to detail, problem-solving abilities, and effective communication skills help ensure accurate data handling and collaboration with cross-functional teams. These skills are vital for ensuring high-quality clinical trial data, regulatory compliance, and the smooth operation of clinical research processes.

What are some common challenges faced by Full Time EDC Programmers during clinical trial projects?

Full Time EDC Programmers often encounter challenges such as integrating complex protocol requirements into electronic data capture (EDC) systems, ensuring data quality and regulatory compliance, and managing tight timelines. Collaboration is key, as programmers frequently work with data managers, clinical teams, and statisticians to address evolving data collection needs and troubleshoot technical issues. Staying up-to-date with evolving EDC software and regulatory standards is essential to effectively support clinical trial operations and ensure smooth data flow.

What is a Full Time EDC Programmer?

A Full Time EDC (Electronic Data Capture) Programmer is a professional who develops, configures, and maintains EDC systems used in clinical trials and research. Their main role is to design electronic case report forms (eCRFs), manage study databases, and ensure accurate data collection and validation. EDC Programmers collaborate closely with clinical teams, data managers, and statisticians to facilitate efficient and compliant data management. Working full time, they focus on supporting multiple studies, troubleshooting issues, and implementing new features or updates to the EDC system.

What is the difference between Full Time Edc Programmer vs Full Time Automation Engineer?

AspectFull Time Edc ProgrammerFull Time Automation Engineer
CredentialsProgramming certifications, technical degreesEngineering degrees, certifications in automation tools
Work EnvironmentElectronics manufacturing, R&D labsIndustrial plants, manufacturing facilities
Industry UsageElectronics, medical devices, aerospaceManufacturing, process industries

Full Time Edc Programmers focus on developing and maintaining embedded control systems for electronic devices, often working in electronics manufacturing environments. Automation Engineers design and implement automated processes in industrial settings. While both roles require technical programming skills and industry knowledge, Edc Programmers specialize in embedded systems, whereas Automation Engineers focus on process automation. The choice depends on your interest in embedded electronics versus industrial automation.

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Full Time Edc Programmer jobs near you
Clinical Trial Specialist

Clinical Trial Specialist

4C Medical Technologies

Maple Grove, MN • On-site

$75K - $100K/yr

Full-time

Posted 11 days ago

Job description

Job Type
Full-time
Description
JOB SUMMARY:
Under general supervision, develops, coordinates, and administers the logistical aspects of clinical trials according to good clinical practice (GCP), good documentation practices (GDP) and standard operating procedures (SOP). Acts as a pivotal point of contact and communication between department staff, clinical sites, as well as vendors.
KEY RESPONSIBILITIES :
1. Oversee and manage operational aspects of clinical trials in conjunction with project teams and in accordance with SOPs, GCP, GDP and specific country regulations, and may prepare clinical trial budgets.
2. Collaborate and partner with a cross-functional team which includes clinical field, site managers, monitors, safety, and others.
3. Build and maintain optimal relationships and effective collaborations with various internal and external parties.
4. Develop, test, and implement clinical tools to provide relevant information for clinical studies management.
5. Manage clinical study site information and documentation.
a. Request, track, review and assure receipt of proper study documentation (IRB approval letters, Signature Pages, Informed Consent materials, signed Clinical Study Agreements, Confidentiality Agreements, etc.).
b. Obtain, review, and file site personnel documentation to ensure site compliance.
c. Develop and distribute clinical study documents (Protocol, Case Report Forms, Informed Consent, Agreements, etc.).
6. Routinely correspond with clinical study sites.
a. Provide timely support as subjects go through the screening process.
b. Promptly answers sites' questions and requests with accuracy.
c. Generate and submit memos and study documents (protocol amendments, newsletters, brochures, etc.) to clinical study sites.
d. Generate, review, and respond to queries the electronic data capture (EDC).
7. Coordinate all information regarding adverse events and ensure all information is received by the internal team and clinical study sites.
8. Maintain accurate records and files of study patient data. Coordinate accurate completion of Case Report Forms in EDC by timely reviewing them and corresponding with sites to update data and/or creating corrective action plans.
9. Coordinate on-site and off-site Investigator, Study Coordinator and Technologist training meetings and conference calls.
10. Provide support to monitoring staff by creating monitoring visit prep packages, answering monitors' questions during visits, and reviewing monitoring visit reports.
11. Order, assemble, and maintain supplies of study materials and equipment (handbooks, Case Report Form books, IDE copies, medical equipment, etc.).
12. Other duties, as assigned by supervisor and/or clinical research project managers.
Requirements
EDUCATION :
Bachelor's degree in engineering, biology, physical sciences, nursing or another related field.
PREFERRED EXPERIENCE :
One plus years of experience in clinical/medical affairs in the medical device industry.
KNOWLEDGE, SKILLS AND ABILITIES:
  • Knowledge of medical terminology and anatomy.
  • Knowledge of FDA guidelines and regulations governing conduct of clinical trials.
  • Detailed knowledge of the documents required for a Regulatory Binder (IRB approvals, Investigator Agreements, CVs, MLs).
  • Strong organizational skills and detail orientation required.
  • Interpersonal and communication skills necessary to interact with study site personnel and physicians.
  • Analytical skills to determine clinical requirements and evaluate software solutions.
  • Intermediate skills in Microsoft Office, Word, and Power Point.
  • Advanced skills in Excel, Access, and clinical database software.
  • Ability to handle multiple priorities in a fast-paced environment.
  • Ability to make independent judgments.
  • Ability to travel as needed up to 20%.

Salary Description
$75,000 to $100,000

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