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Internship Clinical Database Programmer Jobs (NOW HIRING)

Atorus Research

Sr Medidata RAVE Programmer

S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and ...

Collabera

Clinical Data Manager

Irvine, CA · On-site

Work closely with clinical project team and database programmers to provide edit check requirements and specifications at the time of study database development and Post production changes. Ensure ...

Merck & Co.

Senior Statistical Programmer

Rahway, NJ · On-site

Clinical Database Programming, Clinical Trials, Collaborative Development, Data Modeling, Pharmaceutical Development, Project Leadership, Stakeholder Relationship Management, Statistical ...

MSD

Senior Statistical Programmer

North Wales, PA

Clinical Database Programming, Clinical Trials, Collaborative Development, Data Modeling, Pharmaceutical Development, Project Leadership, Stakeholder Relationship Management, Statistical Programming ...

MSD

Senior Statistical Programmer

Rahway, NJ

Clinical Database Programming, Clinical Trials, Collaborative Development, Data Modeling, Pharmaceutical Development, Project Leadership, Stakeholder Relationship Management, Statistical Programming ...

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The CDM will support and/or lead clinical database design, data collection and validation, data ... Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The CDM will support and/or lead clinical database design, data collection and validation, data ... Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ...

eClinical Solutions

Senior Database Engineer

Mansfield, MA · On-site +1

$112K - $152K/yr

Senior Database Engineer eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud, helping life sciences organizations unify, analyze, and unlock the ...

eClinical Solutions

Senior Database Engineer

Mansfield, MA · On-site +1

$112K - $152K/yr

Senior Database Engineer eClinical Solutions is transforming clinical development with elluminate, our Clinical Data Cloud, helping life sciences organizations unify, analyze, and unlock the value of ...

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How much do internship clinical database programmer jobs pay per year?

As of Jul 22, 2026, the average yearly pay for internship clinical database programmer in the United States is $118,962.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $180,000.00 per year, depending on experience, location, and employer.

What does an Internship Clinical Database Programmer do?

An Internship Clinical Database Programmer assists in designing, developing, and managing databases used in clinical trials. They work under the supervision of senior database programmers to ensure data collected from clinical studies is accurate, secure, and compliant with industry standards. Their tasks may include programming data entry screens, validating data, and generating reports, all of which support the integrity of clinical research. This role often involves learning about clinical data management systems and gaining hands-on experience in the pharmaceutical or healthcare industry.

What are the typical responsibilities of an Internship Clinical Database Programmer, and how do they contribute to clinical research projects?

As an Internship Clinical Database Programmer, you will primarily assist in designing, developing, and maintaining clinical databases that capture study data for clinical trials. Your responsibilities may include programming electronic case report forms (eCRFs), validating data entries, running quality control checks, and ensuring data integrity in compliance with regulatory standards. You'll collaborate closely with data managers, biostatisticians, and clinical research associates to resolve data queries and support smooth study operations. This internship offers valuable exposure to the workflow of clinical data management and can serve as a stepping stone to more advanced roles in clinical informatics or data management.

What are the key skills and qualifications needed to thrive as an Internship Clinical Database Programmer, and why are they important?

To thrive as an Internship Clinical Database Programmer, you need a solid understanding of database concepts, programming languages (such as SQL), and a background in life sciences or related fields. Familiarity with clinical data management systems like Medidata Rave or Oracle Clinical, and knowledge of regulatory standards such as CDISC or SDTM, is often required. Strong attention to detail, analytical thinking, and effective communication skills help interns work accurately and collaboratively within project teams. These competencies ensure reliable data handling, regulatory compliance, and successful support of clinical research operations.
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Internship Clinical Database Programmer jobs near you
Infographic showing various Internship Clinical Database Programmer job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $118,962 per year, or $57.2 per hour.

Sr Medidata RAVE Programmer

Atorus Research

Remote

Contractor

Re-posted yesterday

Job description

Sr Medidata RAVE Programmer
Remote from anywhere in the U.S. or Canada
Contract/Corp to Corp
JOB OVERVIEW
The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and provides EDC programming support to the study team in accordance with Atorus and/or sponsor standard operating procedures (SOPs), Good Clinical Practice (GCP), ICH Guidelines and sponsor requirements. The EDC Programmer also assists in technical support for data collection systems.
JOB RESPONSIBILITIES
• Perform study set up and program edit check programming as per the approved specifications with minimal guidance from the line manager or experienced colleagues
• Adhere to project timelines
• Participate in the design and maintenance of the clinical study database per the protocol and any amendments, SOPs, GCP and other regulatory requirements
• Review database specifications and Data Validation Specifications (DVS) and perform programming and configuration activities
• Assist in database release to production activities
• Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented problems in a timely manner, as appropriate for the position. Assist data manager with status reports and listings as necessary
• Advise management on a regular basis on the status and any potential risks or concerns with ongoing projects to ensure timely resolution including any potential issues with resources
• Ensure awareness of project-specific quality and performance standards and ensure that these are adequately documented, communicated, and understood
• Participate in internal and external study team meetings, as required
• Participate in department meetings and initiatives
• Perform other duties as required by the department
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
• 2-4years EDC Programming experience working in pharmaceutical, biotechnology or Contract Research Organization (CRO) preferred
• Course completion of an EDC system training
• Minimum 2-4 years of experience in clinical database design and deployment
• Additional relevant work experience will be considered in lieu of formal qualifications
• Broad knowledge of drug development processes
• Understanding of global clinical development budgets and relationship to productivity targets
• Knowledge of effective clinical data management practices
PREFERRED SKILLS
• Good organizational skills
• Good communication skills, verbal and written
• Detail oriented
• Good computer skills, including Microsoft Office and use of data management systems
• Good problem-solving skills
• Basic knowledge and understanding of EDC and other eTechnologies
• Flexible, team player
• Proven ability to organize and effectively prioritize workload and deliverables

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