Senior Sub-Investigator: Clinical Trials Lead

Velocity Clinical Research, Inc.; Florida; Hybrid; USD 110,000 - 140,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

Company holidays

401(k) with company match

Annual incentive program

Job summary

Velocity Clinical Research, Inc. is seeking a Sub Investigator to lead study teams, oversee patient safety, and ensure accurate data collection across clinical trials. The role requires an MD/DO/NP/PA license and 5+ years of clinical management experience.

You will mentor staff, coordinate trial activities, and ensure compliance with GCP, ICH guidelines, and Velocity SOPs. This position involves hands-on clinical duties, documentation, and collaboration with investigators, sponsors, and CROs to

Qualifications

• Must undertake training and certification required by sponsors/CROs.
• HIPAA privacy and confidentiality practices.
• Professionalism, teamwork, and flexible workload management.
• Effective communication in English (verbal and written).
• Up to 10% travel for meetings and conferences.

Responsibilities

• Lead study teams to execute clinical trials.
• Mentor and train staff in protocol requirements and trial management.
• Develop training strategies and mitigation plans.
• Conduct trials per protocol, GCP, ICH and Velocity SOPs.
• Coordinate startup, vendor management, recruitment, regulatory documents, visits, and data entry; manage adverse events and deviations.

Skills

HIPAA privacy

English communication

Team leadership

Professionalism

Willingness to travel

Education

MD/DO/NP/PA licensed

Job description

Velocity Clinical Research, Inc. is seeking a Sub Investigator to lead study teams, oversee patient safety, and ensure accurate data collection across clinical trials. The role requires an MD/DO/NP/PA license and 5+ years of clinical management experience.

You will mentor staff, coordinate trial activities, and ensure compliance with GCP, ICH guidelines, and Velocity SOPs. This position involves hands-on clinical duties, documentation, and collaboration with investigators, sponsors, and CROs to