Lead Sub-Investigator, Clinical Trials

Velocity-Clinical-Research,-Inc.; Norfolk (NE); On-site; USD 110,000 - 170,000; Full time

Job summary

Velocity Clinical Research, Inc. is seeking a Sub Investigator to oversee the clinical safety of trial participants, collect accurate data, and ensure subject well-being. You will provide essential clinical support to coordinators, principal investigators, and trial staff at Velocity.

The role requires MD/DO/NP/PA licensure and 5+ years of clinical management experience, with up to 10% travel. Strong data integrity, regulatory compliance, and communication skills are essential.

Qualifications

• Must be a licensed MD, DO, NP, or PA.
• Strong understanding of clinical trial conduct and regulatory requirements.
• Ability to communicate effectively in English (verbal and written).
• Up to 10% travel may be required for meetings and conferences.

Responsibilities

• Lead a study team to execute clinical trials in accordance with protocol, GCP, and SOPs.
• Mentor and train staff on trial conduct, protocol requirements, and data quality.
• Coordinate start-up activities, site management, patient recruitment, and regulatory documentation.
• Ensure timely data entry, query resolution, and AE/SAE reporting.
• Maintain confidentiality of subject information and sponsor data.

Skills

HIPAA compliance

English communication

Travel readiness

Education

MD/DO/NP/PA license

Job description

Velocity Clinical Research, Inc. is seeking a Sub Investigator to oversee the clinical safety of trial participants, collect accurate data, and ensure subject well-being. You will provide essential clinical support to coordinators, principal investigators, and trial staff at Velocity.

The role requires MD/DO/NP/PA licensure and 5+ years of clinical management experience, with up to 10% travel. Strong data integrity, regulatory compliance, and communication skills are essential.