Clinical Systems Programmer II: Data & Compliance

Pharmaron Beijing Co. Ltd.

Baltimore (MD)

On-site

USD 60,000 - 70,000

Full time

14 days+
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Benefits offered by this job

Medical, Dental & Vision Insurance
401(k) Retirement Plan
Paid Time Off & Holidays
Employee assistance programs

Job summary

Pharmaron Beijing Co. Ltd. is seeking a Clinical Applications Programmer II to support configuration, programming, validation, and management of electronic systems used to collect and analyze clinical study data.

The role collaborates with cross‑functional teams to ensure systems meet study requirements and regulatory standards. The candidate should have EDC/eSource programming experience, CDISC/CDASH knowledge, and familiarity with 21 CFR Part 11, delivering high‑quality, compliant data and

Qualifications

  • Bachelor's degree or equivalent with 1 year of relevant experience in clinical research, data management, or related field.
  • Experience with eSource/EDC study design and configuration.
  • Familiarity with CDISC standards and 21 CFR Part 11 requirements.

Responsibilities

  • Configure and validate clinical systems (EDC, eSource, LIMS) per study protocols.
  • Create CDISC/CDASH‑compliant eCRFs and study workflows.
  • Develop edit checks and data validation rules; support UAT and defect resolution.

Skills

eSource/EDC design
CDISC/CDASH concepts
JavaScript basics
GCP knowledge
Regulatory/compliance awareness

Education

Bachelor's degree or equivalent + 1 year experience
Associate degree + 2 years experience

Tools

CDMS/EDC systems
SQL/MySQL/PostgreSQL

Job description

Pharmaron Beijing Co. Ltd. is seeking a Clinical Applications Programmer II to support configuration, programming, validation, and management of electronic systems used to collect and analyze clinical study data.

The role collaborates with cross‑functional teams to ensure systems meet study requirements and regulatory standards. The candidate should have EDC/eSource programming experience, CDISC/CDASH knowledge, and familiarity with 21 CFR Part 11, delivering high‑quality, compliant data and

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