Clinical Trials Sub-Investigator Lead

Velocity Clinical Research, Inc.; Norfolk (NE); Hybride; USD 120 000 - 180 000; Plein temps

Avantages offerts par ce poste

Medical insurance

Dental insurance

Vision insurance

Paid time off

Company holidays

401(k) with match

Annual incentive program

Résumé du poste

Velocity Clinical Research, Inc. seeks a Sub Investigator to oversee clinical safety and data quality across multiple trials. You will lead trial teams, mentor staff, manage start-up, recruitment, and regulatory documentation, and ensure adherence to GCP/ICH and sponsor SOPs.

The role requires an MD/DO/NP/PA license and 5+ years of clinical trial management experience. You will collaborate with investigators, sponsors, and CROs to deliver safe, high-integrity data and patient care.

Qualifications

• Must undertake all training and certification required by sponsors and CRO’s to carry out clinical trials within specified timelines.
• Licensed MD, DO, NP, or PA required.
• 5+ years of clinical management experience or equivalent in the clinical research industry.

Responsabilités

• Lead a study team to execute clinical trials.
• Mentor and train staff in trial conduct and protocol requirements.
• Coordinate startup, vendor management, recruitment, and regulatory documents.
• Ensure data entry and query resolution across sponsor/CRO systems.
• Maintain confidentiality of patient information and protect sponsor/Velocity data.

Formation

MD/DO/NP/PA licensure

Description du poste

Velocity Clinical Research, Inc. seeks a Sub Investigator to oversee clinical safety and data quality across multiple trials. You will lead trial teams, mentor staff, manage start-up, recruitment, and regulatory documentation, and ensure adherence to GCP/ICH and sponsor SOPs.

The role requires an MD/DO/NP/PA license and 5+ years of clinical trial management experience. You will collaborate with investigators, sponsors, and CROs to deliver safe, high-integrity data and patient care.