Remote Clinical Data Manager — Data Quality & CDISC

Pharmavise Corporation; Poland; Remote; PLN 120,000 - 180,000; Full time

Benefits offered by this job

Paid holidays

Paid Time Off (PTO)

Medical insurance

Job summary

Pharmavise Corporation is a fully remote Clinical Data Manager position designed to ensure data integrity from collection to database lock. You will collaborate with Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs to support compliant trial execution. The role requires CDISC/SDTM knowledge, ICH-GCP and FDA standards, and experience with Medidata Rave, Oracle InForm, Veeva, and REDCap. A strong data-focused skill set is essential.

Qualifications

• Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or related field.
• 3–5 years of clinical data management experience in pharma/biotech/CRO.
• Experience with EDC platforms (Medidata Rave, Oracle InForm, Veeva, REDCap).
• Strong knowledge of ICH-GCP, FDA regulations, and CDISC standards.
• Excellent analytical, organizational and problem-solving skills.
• Strong communication and collaboration skills across cross-functional teams.
• Experience in global, multi-site clinical trials preferred.

Responsibilities

• Design and review CRFs and EDC systems for accurate data capture.
• Develop data management plans, validation specs, CRF completion guidelines.
• Oversee data cleaning and query resolution with sites and teams.
• Ensure adherence to CDISC standards and regulatory requirements.
• Manage database lock activities and CSR preparation.
• Coordinate with data management vendors and oversight of deliverables.
• Support audit readiness and regulatory inspections when required.

Skills

Data management

CDISC standards

FDA regulations

ICH-GCP

Cross-functional collaboration

Data validation

Query management

Education

Bachelor's in Life Sciences

Advanced degree

Tools

Medidata Rave

Oracle InForm

Veeva

REDCap

Job description

Pharmavise Corporation is a fully remote Clinical Data Manager position designed to ensure data integrity from collection to database lock. You will collaborate with Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs to support compliant trial execution. The role requires CDISC/SDTM knowledge, ICH-GCP and FDA standards, and experience with Medidata Rave, Oracle InForm, Veeva, and REDCap. A strong data-focused skill set is essential.