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Assistant Programmer Jobs in Towson, MD (NOW HIRING)

... * Assist with the development of templates, SOPs, training materials, and standardized practices ... Meet established programming, testing, and study implementation deadlines. * Maintain comprehensive ...

Control Engineer

Baltimore, MD ยท On-site

$83K - $107K/yr

Coverage for the assistant engineer and/or chief engineer in their absence. Qualifications: * High school diploma or GED. * Minimum of 2 years' experience in an automation controls role in an ...

Principal CICS Systems Programmer *** Selected candidate must be willing to work on-site in ... Assist with the installation, maintenance, and user support for InterTest, Abend-Aid, CICS MAPR ...

Control Engineer

Baltimore, MD ยท On-site

$83K - $107K/yr

Coverage for the assistant engineer and/or chief engineer in their absence. Qualifications: * High school diploma or GED. * Minimum of 2 years' experience in an automation controls role in an ...

Mainframe z/OS System Programmer

Columbia, MD ยท Remote

$56.25 - $71.75/hr

Experience monitoring and managing security reporting ensuring systems are compliant. * Assist systems programmers in the design and management of ACF2 / RACF / TSS for all regions and LPARs.

... Assist in project artifact documentation in business requirement documents, functional specs, flow charts and system architectures source to target mappings etc. o Enable governments plan, design ...

Showing results 21-40

Assistant Programmer information

See Towson, MD salary details

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How much do assistant programmer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for assistant programmer in Towson, MD is $37.88, according to ZipRecruiter salary data. Most workers in this role earn between $24.66 and $49.28 per hour, depending on experience, location, and employer.

What is an assistant programmer?

Assistant Programmers are entry-level professionals who support the development, testing, and maintenance of software applications. They typically work under the supervision of senior programmers or software engineers, helping to write code, debug programs, and document software processes. Their main role is to assist with routine programming tasks and learn industry best practices, making this position a common starting point for a career in software development.

What are the key skills and qualifications needed to thrive as an assistant programmer?

To thrive as an Assistant Programmer, you need foundational knowledge in programming languages (such as Java, Python, or C++), software development fundamentals, and typically a degree or coursework in computer science or a related field. Familiarity with version control systems (like Git), integrated development environments (IDEs), and debugging tools is highly valuable. Strong problem-solving abilities, attention to detail, and effective communication skills help you collaborate with team members and deliver quality code. These skills and qualities are crucial for efficiently supporting software projects and ensuring reliable, maintainable applications.

What are some typical challenges faced by assistant programmers when joining a new development team?

Assistant Programmers often encounter challenges such as adapting to the team's coding standards, learning new tools or frameworks, and understanding the existing codebase. It can also be a learning curve to effectively communicate with senior developers and contribute to collaborative projects. However, most teams provide mentorship, documentation, and code reviews to help new team members integrate smoothly and build confidence in their technical and interpersonal skills.

What is the difference between Assistant Programmer vs Junior Developer?

AspectAssistant ProgrammerJunior Developer
Required CredentialsTypically an associate degree or diploma in computer science or related fieldSimilar, often an entry-level role with comparable educational background
Work EnvironmentSupportive team, assisting senior programmers in coding and testingHands-on coding, debugging, and developing software applications
Employer & Industry UsageCommon in IT firms, software companies, and tech departmentsUsed across similar industries, often interchangeable with Assistant Programmer in job listings

In summary, Assistant Programmers and Junior Developers share similar educational backgrounds and work environments. The main difference lies in their roles: Assistant Programmers typically support and assist senior staff, while Junior Developers are more involved in actual coding and development tasks. Both positions serve as entry points into the software development industry.

How to get a job as an assistant programmer with no experience?

To get a job as an assistant programmer with no experience, focus on building foundational skills in programming languages like Python or Java through online courses or tutorials. Create a portfolio of small projects to demonstrate your abilities, and consider internships or entry-level positions that offer on-the-job training to gain practical experience.

What are the most commonly searched types of Programmer jobs in Towson, MD?

The most popular types of Programmer jobs in Towson, MD are:

What job categories do people searching Assistant Programmer jobs in Towson, MD look for?

The top searched job categories for Assistant Programmer jobs in Towson, MD are:

What cities near Towson, MD are hiring for Assistant Programmer jobs?

Cities near Towson, MD with the most Assistant Programmer job openings:

Infographic showing various Assistant Programmer job openings in Towson, MD as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 22% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $78,780 per year, or $37.9 per hour.

Clinical Applications Programmer II

Pharmaron

Baltimore, MD โ€ข On-site

$60K - $70K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 19 days ago


Job description

Position: Clinical Applications Programmer II
Salary Range: $60,000-70,000
Location: Baltimore, MD
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
What You'll Do
We are seeking a Clinical Systems Programmer II to support the configuration, programming, validation, and ongoing management of electronic systems used to collect, process, and analyze clinical study data. This role will work closely with Clinical Data Management, Clinical Operations, Laboratory, IT, Regulatory, project teams, and study sponsors to ensure clinical systems are designed, tested, documented, and maintained in accordance with study requirements and industry standards.
The ideal candidate combines clinical research knowledge, EDC/eSource programming experience, clinical database design, and familiarity with CDISC standards and 21 CFR Part 11 requirements. This is a hands-on role for someone who enjoys solving complex system and data challenges while ensuring high-quality, compliant clinical data collection.
Key Responsibilities
  • Configure eSource, EDC, Laboratory Information Systems, and other clinical systems based on study protocols, laboratory manuals, pharmacy manuals, and related study documentation.
  • Create and maintain CDISC/CDASH-compliant eCRFs, study workflows, dynamic forms, and conditional logic.
  • Program screening, inpatient, and follow-up workflows in accordance with study protocols and source templates.
  • Develop and maintain edit checks and data validation rules using logic operators to authenticate data entered into electronic forms.
  • Utilize basic JavaScript or similar programming languages to create and modify methods, edit checks, and study-specific functionality.
  • Develop User Acceptance Testing (UAT) documentation and support Clinical Information Specialists in completing UAT activities.
  • Troubleshoot system issues, investigate defects, and implement appropriate solutions.
  • Participate in meetings with Project Managers, clinical and laboratory leaders, and study sponsors to ensure systems capture, process, and report required study data.
  • Collaborate with Clinical Systems leadership, IT, and Regulatory teams on system upgrades, implementation timelines, and validation activities.
  • Assist with the development of templates, SOPs, training materials, and standardized practices to improve efficiency and minimize study-specific build time.
  • Meet established programming, testing, and study implementation deadlines.
  • Maintain comprehensive documentation to support audit readiness and regulatory compliance.
  • Provide system training and ongoing technical support to subject matter experts and end users.
  • Serve as the primary systems point of contact for assigned clinical studies.
  • Work independently while collaborating effectively with the Data Management team and cross-functional stakeholders.
  • Support compliance with Good Clinical Practice (GCP), CDISC standards, 21 CFR Part 11, and applicable clinical research requirements.

What We're Looking For
Required Qualifications
  • High school diploma plus 4 years of relevant experience in at least two of the following areas; OR
  • Associate degree/equivalency (60+ college credit hours) plus 2 years of relevant experience in at least two of the following areas; OR
  • Bachelor's degree/equivalency (120+ college credit hours) plus 1 year of relevant experience in at least two of the following areas:
    • Clinical research, life sciences, public health, or related field
    • eSource or EDC study design and configuration
    • Application support
    • System validation and User Acceptance Testing
    • CDISC terminology and standards
    • JavaScript or other programming languages

Knowledge & Skills
  • Understanding of Good Clinical Practice (GCP) and clinical research processes.
  • Working knowledge of CDISC standards, including CDASH and SDTM concepts.
  • Experience designing data collection solutions that support standardized clinical trial data capture and reporting.
  • Basic proficiency with JavaScript or a similar programming language.
  • Strong analytical and critical-thinking skills with the ability to troubleshoot complex system and data issues.
  • Strong quality-control and testing skills.
  • Ability to analyze system requirements and evaluate how system changes may impact clinical study operations and data.
  • Excellent communication and active-listening skills.
  • Ability to manage multiple priorities and meet programming and testing deadlines.
  • Ability to work independently and collaboratively across functional teams.
  • Strong attention to detail and commitment to data quality and regulatory compliance.

Preferred Qualifications
  • Master's degree in Computer Science, Health Informatics, Clinical Research, Data Science, or a related field.
  • Industry certifications in clinical research, data management, EDC systems, programming, or related disciplines.
  • Experience with Active Directory administration.
  • Network troubleshooting experience.
  • Application support experience.
  • Laboratory, pharmacy, or clinical application experience.
  • Web design, programming, and/or web administration experience.
  • Experience with MySQL, PostgreSQL, Microsoft SQL, Oracle, and/or Microsoft Access.
  • Laboratory, pharmacy, or clinical management experience.

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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