Lead Sub-Investigator, Clinical Trials

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

Job summary

Velocity Clinical Research, Inc. is seeking a Sub Investigator to oversee clinical safety and data collection for patients in trials. You will support clinicians and staff to ensure high-quality data and patient welfare throughout the study.

As a lead, you will mentor teams, ensure adherence to protocol, GCP/ICH, and Velocity SOPs, and coordinate across startups, vendors, and sponsors to deliver compliant trial results.

Qualifications

• Must hold an MD, DO, NP, or PA license.
• 5+ years of clinical management experience in clinical research.
• Ability to communicate effectively in English.
• Must undertake training/certification required by sponsors and CROs.
• Up to 10% travel as needed.

Responsibilities

• Lead a study team to execute clinical trials.
• Train staff in trial conduct, protocol requirements, and trial management.
• Coordinate startup, vendor management, subject recruitment, and data collection.
• Ensure data entry, query resolution, and adverse event reporting per protocol.
• Maintain regulatory documents and ensure patient safety.

Skills

Clinical trial management

Leadership

English communication

HIPAA privacy

Travel up to 10%

Education

MD/DO/NP/PA license

Job description

Velocity Clinical Research, Inc. is seeking a Sub Investigator to oversee clinical safety and data collection for patients in trials. You will support clinicians and staff to ensure high-quality data and patient welfare throughout the study.

As a lead, you will mentor teams, ensure adherence to protocol, GCP/ICH, and Velocity SOPs, and coordinate across startups, vendors, and sponsors to deliver compliant trial results.