Lead Sub-Investigator: Trials Leadership & Mentorship

Velocity Clinical Research, Inc.; Puławy; On-site; PLN 120,000 - 180,000; Full time

Job summary

Velocity Clinical Research in Puławy, Poland, is seeking a Sub Investigator to oversee clinical safety and data accuracy across trials. You will mentor coordinators, ensure protocol adherence, and coordinate regulatory documents under GCP/ICH and Velocity SOPs.

The role requires MD/DO/NP/PA licensure, strong English communication, and up to 10% travel. Join a team focused on high-quality data and exemplary patient care across studies.

Qualifications

• Must undertake all training and certification required by sponsors and CROs.
• Proven ability to manage clinical trials in accordance with protocol and GCP.
• Demonstrated professionalism, teamwork and flexibility in fast-paced environments.

Responsibilities

• Lead a study team to execute clinical trials while ensuring patient safety.
• Mentor and train staff in trial conduct, protocol requirements and trial management.
• Study startup, vendor management, subject recruitment and regulatory document collection.
• Ensure data capture accuracy, timely entry, and resolution of queries.
• Maintain compliance with HIPAA, GCP/ICH and Velocity SOPs; report adverse events as required.

Skills

English communication

Clinical trial management

HIPAA privacy compliance

Data handling

Travel readiness

Education

Licensed MD/DO/NP/PA

Job description

Velocity Clinical Research in Puławy, Poland, is seeking a Sub Investigator to oversee clinical safety and data accuracy across trials. You will mentor coordinators, ensure protocol adherence, and coordinate regulatory documents under GCP/ICH and Velocity SOPs.

The role requires MD/DO/NP/PA licensure, strong English communication, and up to 10% travel. Join a team focused on high-quality data and exemplary patient care across studies.