Lead Sub-Investigator – Clinical Trials Expert

Velocity-Clinical-Research,-Inc.; Puławy; On-site; PLN 180,000 - 320,000; Full time

Job summary

Velocity Clinical Research is seeking a Sub Investigator to oversee clinical trial activities in Puławy, Poland. The role involves leading a study team, mentoring staff, and ensuring patient safety, data integrity, and adherence to protocol, GCP, and SOPs.

The ideal candidate is a licensed MD/DO/NP/PA with 5+ years in clinical management or equivalent industry experience, willing to travel up to 10% and collaborate with sponsors, CROs, and vendors to drive trial success.

Qualifications

• Must undertake all training and certification required by sponsors and CROs to carry out clinical trials.
• Professionalism and integrity in all actions; teamwork and flexibility to get the work done.
• Ability to communicate effectively in English (verbal and written).
• Up to 10% travel for meetings and conferences as needed.

Responsibilities

• Lead a study team to execute clinical trials in accordance with protocol and GCP.
• Mentor and train staff in trial conduct and protocol requirements.
• Coordinate start-up, vendor management, recruitment, and regulatory documents.
• Ensure data entry, query resolution, and reporting of adverse events.
• Develop communication strategies to protect patient safety and data integrity.

Skills

Training & Certification

English communication

Teamwork

Flexibility

Travel up to 10%

Education

MD/DO/NP/PA license

Job description

Velocity Clinical Research is seeking a Sub Investigator to oversee clinical trial activities in Puławy, Poland. The role involves leading a study team, mentoring staff, and ensuring patient safety, data integrity, and adherence to protocol, GCP, and SOPs.

The ideal candidate is a licensed MD/DO/NP/PA with 5+ years in clinical management or equivalent industry experience, willing to travel up to 10% and collaborate with sponsors, CROs, and vendors to drive trial success.