Remote Clinical Research Associate – Study Maintenance

Pharmavise Corporation; Poland; Remote; PLN 297,000 - 408,000; Full time

Job summary

Pharmavise Consulting Corporation seeks experienced Clinical Research Associates (CRAs) to provide surge capacity support for ongoing clinical projects in a fully remote role. You will support study maintenance, data lock, closeout activities, and serve as a primary liaison with internal teams and external partners.

The role emphasizes collaboration, regulatory compliance, and data integrity across safety, biomarkers, PK/ADA, imaging, and device data, with a focus on efficient operations rather

Qualifications

• Bachelor’s degree in a relevant field.
• 6+ years in clinical research or a related industry.
• 3+ years in project management or a related role.
• Experience in pharma, diagnostics, or CRO environments.
• Proficiency with Excel for data tracking and reporting.
• Experience with CTMS tools (Medidata RAVE, Veeva Vault, Oracle InForm) and eTMF systems.

Responsibilities

• Oversee study maintenance, data lock, closeout, document review, and budget monitoring.
• Act as the primary liaison between internal study teams and external third-party organizations (TPOs).
• Track and monitor safety, biomarker, PK, ADA, imaging data, and connected device data.
• Manage and track clinical queries to ensure timely resolution.
• Coordinate with business partners and TPOs to ensure compliance with study requirements.

Skills

Clinical research

Project management

GCP knowledge

Data tracking

Education

Bachelor’s degree in a relevant field

Tools

Medidata RAVE

Veeva Vault

Oracle InForm

eTMF systems

Job description

Pharmavise Consulting Corporation seeks experienced Clinical Research Associates (CRAs) to provide surge capacity support for ongoing clinical projects in a fully remote role. You will support study maintenance, data lock, closeout activities, and serve as a primary liaison with internal teams and external partners.

The role emphasizes collaboration, regulatory compliance, and data integrity across safety, biomarkers, PK/ADA, imaging, and device data, with a focus on efficient operations rather