Lead Sub-Investigator - Clinical Trials & Data Quality

Velocity-Clinical-Research,-Inc.; Zamość; On-site; PLN 180,000 - 280,000; Full time

Job summary

Velocity Clinical Research is seeking a Sub Investigator to oversee clinical safety and data accuracy in trials, supporting coordinators and principal investigators. The role emphasizes adherence to GCP, ethical standards, and robust data management.

The Sub Investigator provides essential clinical support, ensures patient well-being, and collaborates with sponsors and CROs to maintain study integrity and timely data delivery.

Qualifications

• Must complete training and sponsor/CRO certifications within timelines.
• Safe handling of data and records per privacy requirements.
• Demonstrates professionalism, teamwork, and flexibility.
• Ability to communicate effectively in English (spoken and written).
• Up to 10% travel for meetings and conferences.

Responsibilities

• Lead study team to execute clinical trials.
• Mentor staff in trial conduct and protocol requirements.
• Coordinate startup, vendor management, recruitment, and regulatory documents.
• Ensure data entry, query resolution, and adverse event reporting per protocol.

Skills

Training compliance

Data privacy (HIPAA)

Professional conduct

English communication

Travel readiness

Education

MD/DO/NP/PA license

5+ years clinical management experience

Job description

Velocity Clinical Research is seeking a Sub Investigator to oversee clinical safety and data accuracy in trials, supporting coordinators and principal investigators. The role emphasizes adherence to GCP, ethical standards, and robust data management.

The Sub Investigator provides essential clinical support, ensures patient well-being, and collaborates with sponsors and CROs to maintain study integrity and timely data delivery.