Sub Investigator – Clinical Research
Company: Velocity Clinical Research
Employment Type: Full-Time
Category: Clinical Research / Medical Affairs
Job ID: 2026-3302
Sub Investigator Jobs in Clinical Research | MD / DO / NP / PA Careers
Velocity Clinical Research, a fully integrated research site organization, is seeking a qualified Sub Investigator (Sub-I) to support the execution of clinical trials and ensure patient safety, regulatory compliance, and data integrity. This full-time position is ideal for licensed medical professionals with clinical research experience who are passionate about advancing innovative medical treatments.
The Sub Investigator plays a critical role in protecting study participants, ensuring protocol compliance, and supporting Principal Investigators and clinical research teams in the successful delivery of clinical trials.
Position Overview
The Sub Investigator is responsible for overseeing the clinical safety of patients enrolled in clinical trials, ensuring accurate data collection, and maintaining compliance with ICH-GCP, FDA regulations, HIPAA requirements, and company SOPs.
This role combines clinical oversight, study leadership, regulatory coordination, and project management to ensure trials are conducted efficiently and ethically.
Key Responsibilities
Clinical Trial Oversight & Execution
Conduct and manage clinical trials in accordance with approved protocols, ICH-GCP guidelines, and regulatory requirements
Provide medical oversight to ensure patient safety and well-being throughout the study
Evaluate and pre-screen potential subjects for eligibility (phone and in-person assessments)
Perform clinical procedures within scope of practice (e.g., drug administration, ECG, phlebotomy, lab processing, fibroscan)
Manage protocol amendments, study start-up, and close-out activities
Safety & Regulatory Compliance
Monitor, document, and report adverse events (AEs), serious adverse events (SAEs), and protocol deviations
Ensure timely and accurate data entry into sponsor portals and resolution of queries
Maintain strict adherence to HIPAA and confidentiality standards
Oversee regulatory documentation submission to sponsors and IRBs
Study Leadership & Team Management
Lead and mentor clinical study teams
Train staff on protocol requirements, compliance standards, and documentation practices
Develop training strategies and quality control measures
Ensure proper delegation of authority and documentation of staff qualifications
Foster teamwork, professionalism, and ethical conduct
Project & Operational Management
Develop recruitment strategies in collaboration with patient recruitment teams
Apply risk management principles to enhance study quality and efficiency
Incorporate understanding of product development lifecycle and protocol design
Manage vendor coordination and study timelines
Communicate effectively with sponsors, CROs, leadership, and study teams
Participate in professional meetings and project-related travel (up to 10%)
Experience Required
Minimum 5+ years of clinical management experience or equivalent experience in the clinical research industry
Proven experience conducting or overseeing clinical trials
Experience in patient safety monitoring and regulatory compliance
Prior leadership or team management experience in research settings preferred
Educational & Licensing Requirements
Must be a licensed MD, DO, Nurse Practitioner (NP), or Physician Assistant (PA)
Active and unrestricted state medical license required
Completion of sponsor and CRO-required training and certifications
Required Skills & Competencies
Strong understanding of ICH-GCP guidelines and FDA regulatory requirements
Knowledge of clinical trial lifecycle and protocol design
Demonstrated ability to ensure data integrity and audit readiness
Excellent verbal and written communication skills in English
Strong leadership and mentorship abilities
Ability to manage multiple studies and deadlines simultaneously
High level of professionalism, integrity, and patient-centered focus
Strong organizational and problem-solving skills
Physical & Work Requirements
Ability to sit for prolonged periods and work on a computer
Ability to lift up to 15 pounds when necessary
Travel up to 10% for project meetings, conferences, or sponsor engagements
Benefits
Velocity Clinical Research offers a competitive compensation and benefits package, including:
Medical, dental, and vision insurance
Paid time off and company holidays
401(k) retirement plan with company match
Annual incentive program
Career advancement opportunities within a growing research network
Why Join Velocity Clinical Research?
This role provides medical professionals with the opportunity to:
Contribute directly to innovative clinical research programs
Ensure patient safety in cutting-edge therapeutic studies
Gain leadership experience in clinical trial operations
Work in an integrated research site network committed to quality and excellence
Keywords for Search Optimization
Sub Investigator Jobs, Clinical Research Sub Investigator, MD Clinical Trial Jobs, NP Clinical Research Jobs, PA Clinical Trials Careers, Clinical Trial Physician Jobs, ICH GCP Clinical Research Careers, Clinical Research Site Leadership Jobs, Medical Investigator Jobs
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