ClinSpark Programmer I
Pharmaron
Summary
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.
Job description
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
Requirements
- 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: Web Design, Programming, and/or Administration
- Preferred: MySQL, PostgreSQL, Microsoft SQL, Oracle, and/or Access
- Preferred: Laboratory, Pharmacy, or Clinical Management Experience
Benefits
- Medical, Dental & Vision
- 401(k) Matching
- Paid Time Off
- Paid Sick Leave
- Company Holidays
- Health Savings Account
- Flexible Spending Accounts
- Life Insurance
- AD&D Insurance
- Short-Term Disability
- Long-Term Disability
- Employee Assistance Program
- Mental Health Resources
- Wellness Programs
- Fertility Support
- Maternity Resources
- Professional Development
Company overview
Pharmaron is a premier global life sciences service provider founded in 2004, offering comprehensive research, development, and manufacturing services throughout the entire drug discovery and development process. As a leading Contract Research Organization (CRO) and Contract Development and Manufacturing Organization (CDMO), Pharmaron provides integrated solutions across multiple therapeutic modalities including small molecules, biologics, and cell and gene therapy (CGT) products. The company's extensive service portfolio encompasses synthetic and medicinal chemistry, biology services, DMPK (drug metabolism and pharmacokinetics), pharmacology, toxicology, radiochemistry, CMC (chemistry, manufacturing, and controls), and clinical development services. With over 10,000 employees worldwide and facilities across China, the United States, and Europe, Pharmaron supports pharmaceutical and biotechnology companies in accelerating their R&D programs from early discovery through commercial manufacturing. The company is publicly listed on both the Shenzhen and Hong Kong stock exchanges and maintains a strong commitment to scientific excellence, regulatory compliance, and technological innovation in the life sciences sector.