On-site Clinical Informatics Specialist (ClinSpark)

Pharmaron Beijing Co. Ltd.; Baltimore (MD); On-site; USD 33,000 - 41,000; Full time

Benefits offered by this job

Medical, Dental & Vision Insurance

401(k) Retirement Plan

Paid Time Off (PTO)

Health Savings Account (HSA)

Job summary

Pharmaron is recruiting an on-site Clinical Informatics Specialist in Baltimore. You will translate study protocols into ClinSpark configurations, identify data collection points, and ensure accurate data capture for robust study builds.

The role requires a Bachelor of Science in a related field and 1 year of CRC experience or 3 years in clinical research. You will collaborate with Clinical Operations, Biostatistics, and Data Management to support compliant study execution.

Qualifications

• Bachelor of Science in related field required.
• 1 year as a Clinical Research Coordinator or 3 years of experience in clinical research.

Responsibilities

• Configure ClinSpark electronic case report forms (eCRFs) from study protocols.
• Identify key data collection points and ensure accurate data capture for study builds.
• Coordinate with Clinical Applications Team to address protocol changes and maintain compliance.
• Perform UAT for ClinSpark and review study data collection forms against protocols.
• Serve as liaison to other departments for eCRF modifications during the study build.

Skills

Clinical Research Coordination

Data management

Education

Bachelor of Science in related field

Job description

Pharmaron is recruiting an on-site Clinical Informatics Specialist in Baltimore. You will translate study protocols into ClinSpark configurations, identify data collection points, and ensure accurate data capture for robust study builds.

The role requires a Bachelor of Science in a related field and 1 year of CRC experience or 3 years in clinical research. You will collaborate with Clinical Operations, Biostatistics, and Data Management to support compliant study execution.