ClinSpark Programmer I

Pharmaron; Baltimore (MD); On-site; USD 60,000 - 70,000; Full time

Benefits offered by this job

Medical, Dental & Vision Insurance

401(k) Retirement Plan

Job summary

Pharmaron is seeking a ClinSpark Programmer I in Baltimore, MD to support the ClinSpark system across clinical studies. You’ll configure data collection systems, develop eCRFs, and help ensure accurate data capture and reporting.

The role requires basic JavaScript skills, attention to study workflows, and collaboration with data management and clinical teams to meet deadlines and ensure audit readiness.

Qualifications

• Must have educational background in clinical research, life sciences, public health, or related field.
• Experience with eSource or EDC study design.
• Applications support experience and CDISC terminology familiarity.

Responsibilities

• Configure eSource and clinical systems per study protocols.
• Create CDISC/CDASH compliant eCRFs and study workflows.
• Program screening, inpatient and follow-up workflows per protocol.
• Use logic to create edit checks and validate data in forms.
• Use JavaScript for basic methods and UI enhancements.
• Create UAT docs and assist with UAT activities.
• Troubleshoot system issues and resolve defects.
• Attend meetings with PMs and sponsors to ensure data reporting.
• Meet programming and testing deadlines.
• Support audit readiness with documentation.
• Provide system training to SMEs and end users.
• Act as main study contact and work with Data Management cross-functionally.

Skills

Attention to detail

Analytical thinking

Communication skills

Team collaboration

Education

High School Diploma + 4 years experience in 2 areas

Associate's degree/equivalency (60+ credits) + 2 years

Bachelor's degree/equivalency (120+ credits) + 1 year

Tools

CDISC/CDASH

eCRF design

JavaScript

UAT documentation

Job description

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.

Position: ClinSpark Programmer I

Salary Range: $60K-$70K

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.

What You'll Do

The ClinSpark Programmer I is responsible for the routine configuration and programming of the ClinSpark system, which supports the collection, processing, and analysis of clinical study data. This role will help ensure the system is properly configured to meet study requirements while providing end-to-end user support and troubleshooting. Additional responsibilities include assisting with staff training, addressing system-related questions, and supporting the effective use of ClinSpark across clinical study operations.

Key Responsibilities

• Configure eSource, Laboratory Information Systems, and other clinical systems based upon the requirements provided in study protocols, lab manuals, pharmacy manuals, and other study design documents.
• Create and maintain CDISC/CDASH compliant eCRFs, and study workflows with dynamic forms, and conditional logic.
• Program screening, inpatient, and follow-up workflows in accordance with study protocol and source template.
• Use logic operators to create edit checks and authenticate data entered into electronic forms.
• Use basic JavaScript to create methods
• Create User Acceptance Testing (UAT) documentation and assist Clinical Information Specialists to perform UAT activities.
• Troubleshoot system issues and resolve study build defects.
• Attend meetings with project managers, clinical and laboratory leaders, and study sponsors to ensure applications are capturing and reporting all required study data.
• Adhere to programming and testing deadlines.
• Support audit readiness through comprehensive documentation.
• Provide system training and support to departmental subject matter experts and end users.
• Act as main point of contact for assigned studies.
• Ability to work independently and collaboratively within Data Management department and cross-functionally.

What We're Looking For

• High School Diploma + 4 years of experience in at least 2 of the following areas OR Associate's degree/equivalency (60 or more college credit hours) + 2 years experience in at least 2 of the following areas OR Bachelor's degree/equivalency (120 or more college credit hours) + 1 year experience in at least 2 of the following areas:
  • Education in Clinical research, life sciences, public health, or other relevant field
  • Study design of eSource or EDC systems
  • Applications Support
  • CDISC terminology

Preferred Education And Experience

• Web Design, Programming, and/or Administration
• MySQL, PostgreSQL, Microsoft SQL, Oracle, and/or 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:

• 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

As an Equal Employment Opportunity and Affinitive 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.

About Pharmaron

Pharmaron (Stock Code: 300759.SZ/3759.HK) is a premier R&D 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 19,000 employees, and operations in China, the U.S., and the U.K., Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China.

Pharmaron is proud to be an Equal Employment Opportunity and Affinitive Action employer.