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 with employer  

Generous PTO & Holidays

HSA contributions

Life Insurance & AD&D

EAP & wellness programs

Fertility support

Career development opportunities

Job summary

Pharmaron is seeking a ClinSpark Programmer I to support the ClinSpark system for clinical study data collection, processing, and analysis in Baltimore, MD. You’ll configure systems to meet study requirements, provide end-to-end user support, and help with staff training across clinical study operations.

Responsibilities include configuring eSource/LIS, creating CDISC/CDASH compliant eCRFs, programming workflows, and developing UAT documentation while ensuring timely delivery and audit readiness.

Qualifications

• High School Diploma with 4 years in at least 2 areas or an Associate’s degree with 2 years in 2 areas or a Bachelor’s degree with 1 year in 2 areas.
• Education in clinical research, study design of eSource/EDC systems, CDISC terminology, and Applications Support.

Responsibilities

• Configure ClinSpark and related systems per study protocols.
• Create CDISC/CDASH eCRFs and study workflows with dynamic forms.
• Program screening and workflows per protocol and templates.
• Develop edit checks and basic JavaScript methods for data validation.
• Create UAT docs and assist with UAT activities.
• Troubleshoot issues and support audit readiness and cross-functional teams.

Education

Clinical research education

eSource/EDC study design

CDISC terminology

Applications Support

Tools

MySQL

PostgreSQL

MS SQL

Oracle

Access

Job description

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.

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 www.pharmaron.com.

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 Affirmtive 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.