Clinical Trials Sub-Investigator Lead

Velocity Clinical Research, Inc.; Polska; Hybrid; PLN 180,000 - 260,000; Full time

Job summary

Velocity Clinical Research, Inc. seeks a Sub Investigator to oversee the clinical safety and data integrity of assigned trials, mentor staff, and ensure protocol adherence and regulatory compliance.

The requirements include licensed MD/DO/NP/PA, 5+ years of clinical management in trials, and strong English communication. Travel up to 10% may be required to support investigators and study-site coordinators while maintaining regulatory standards.

Qualifications

• Must undertake all training and certification required by sponsors and CROs to carry out clinical trials within specified timelines.
• Safe handling of data and records regarding privacy and confidentiality, per HIPAA requirements.
• Ability to communicate effectively in English (both verbal and written).
• Up to 10% travel, as needed, for project team meetings, client presentations and other professional meetings/conferences as needed.

Responsibilities

• Lead a study team to execute clinical trials.
• Mentor and train staff in the conduct of clinical trials, protocol requirements, communication, and trial management skills.
• Create training strategies and mitigation plans.
• Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs.
• Develop Quality Control strategies for team member projects.

Skills

Clinical trial leadership

Data integrity

Regulatory compliance

Mentoring staff

English communication

Education

MD/DO/NP/PA license

Job description

Velocity Clinical Research, Inc. seeks a Sub Investigator to oversee the clinical safety and data integrity of assigned trials, mentor staff, and ensure protocol adherence and regulatory compliance.

The requirements include licensed MD/DO/NP/PA, 5+ years of clinical management in trials, and strong English communication. Travel up to 10% may be required to support investigators and study-site coordinators while maintaining regulatory standards.