Lead Sub-Investigator, Clinical Trials & Data Quality

Velocity-Clinical-Research,-Inc.; Florida; On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

401(k) with company match

Annual incentive program

Job summary

Velocity Clinical Research seeks a Sub Investigator to oversee the clinical safety of study participants, collect and verify data, and protect patient well-being across trials. You will support coordinators, principal investigators, and staff to ensure protocol adherence and high-quality data.

Responsibilities include leading trials, mentoring staff, managing regulatory documents, adverse event reporting, data entry, and communication with sponsors and CROs, in line with Velocity SOPs and

Qualifications

• Must be a licensed MD, DO, NP, or PA.
• 5+ years of clinical management experience in the clinical research industry.
• Experience leading trials and ensuring GCP/ICH compliance.

Responsibilities

• Serve as leader of a study team to execute clinical trials.
• Mentor and train staff in trial conduct, protocol requirements, communication, and trial management skills.
• Create training strategies and mitigation plans.
• Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs.
• Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment and regulatory document collection.
• Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study.
• Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols.
• Communicate effectively with coworkers, leadership, sponsors, CROs, and vendors.
• Ensure good documentation practices are applied by team members and data is accurately entered and queries resolved.
• Maintain confidentiality of patient information and Velocity confidential information.
• Develop escalation strategies to ensure patient safety and proper reporting of adverse events.
• Ensure data is entered into sponsor data portals and queries resolved in a timely manner.
• Ensure staff are trained and documents are properly stored.
• Prepare and submit regulatory documents to Sponsors and IRBs as required.

Skills

Clinical trial leadership

Team mentorship

Regulatory compliance

English communication

Education

MD/DO/NP/PA

Job description

Velocity Clinical Research seeks a Sub Investigator to oversee the clinical safety of study participants, collect and verify data, and protect patient well-being across trials. You will support coordinators, principal investigators, and staff to ensure protocol adherence and high-quality data.

Responsibilities include leading trials, mentoring staff, managing regulatory documents, adverse event reporting, data entry, and communication with sponsors and CROs, in line with Velocity SOPs and