Sub-Investigator

Be Well Clinical Studies • Round Rock, TX

5d • Onsite

About The Position

At Be Well Clinical Studies, we are dedicated to advancing medical research and improving patient outcomes. We’re currently seeking a highly motivated and detail-oriented Sub-Investigator to join our growing team. This role plays a critical part in the success of our clinical trials, directly impacting participant safety and the integrity of our study operations. This opportunity may be structured as either a full-time employee position or a full-time contractor engagement, depending on candidate preference, qualifications, and study needs. About the Role: As a Sub-Investigator (Sub-I), you will support the Principal Investigator in the compliant and ethical execution of clinical trials while collaborating closely with the broader clinical team. You will be responsible for safeguarding the well-being of study participants, performing delegated medical duties such as physical exams and medical oversight, and ensuring strict adherence to study protocols. This role is integral to maintaining clinical integrity, verifying protocol compliance, and contributing to high-quality data collection throughout the trial process. By upholding the highest standards of care and research excellence, you will directly impact participant safety and study success.

Requirements

• Physician (MD or DO)
• Physician Assistant
• Nurse Practitioner

Nice To Haves

• Research experience is a plus, but not required
• Specialized positions are also available for clinical personnel with a master’s degree in a medical discipline.

Responsibilities

• Participant Safety & Medical Oversight – Conduct physical exams and provide clinical supervision for study-related procedures such as vaccinations, infusions, and other medically attended visits.
• Eligibility Assessment – Review medical history and concomitant medications to evaluate inclusion/exclusion criteria and verify participant eligibility.
• Informed Communication – Address subject questions regarding the investigational product (IP), study protocols, and health-related concerns to ensure clarity and understanding.
• Protocol Adherence – Follow investigator-assigned responsibilities aligned with protocol-specific requirements and study milestones.
• Training & Compliance – Maintain current GCP certification and complete study-specific training; adhere to regulatory, ethical, and institutional standards throughout the trial.
• Team Collaboration – Work in close coordination with the PI, Medical Director, Chief Scientific Officer, Site Manager, and broader clinical research team to support smooth study operations and compliance

Benefits

• A mission-driven team passionate about health equity and access
• Opportunities for professional development and career growth in clinical research
• Collaborative and supportive work environment with strong leadership engagement

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree