Medical Director – Ultrasound & Contrast Research Study
Position Overview We are seeking a physician to provide medical leadership and clinical oversight for a research program evaluating ultrasound-based imaging of cerebral blood flow and neural activity in volunteer participants. The Medical Director will work with the research team, Wellness MD Group’s clinical leadership, and nursing staff to develop clinical protocols, establish participant eligibility criteria, oversee contrast-agent administration, and support participant safety. The physician may also serve as Principal Investigator (PI), subject to review and acceptance of the study and the responsibilities associated with that appointment. Key Responsibilities: Clinical Protocol Development Review the study objectives, supporting literature, proposed ultrasound procedures, and contrast-administration methods. Develop and approve clinical protocols, including participant screening, inclusion and exclusion criteria, contraindications, monitoring, and discharge criteria. Evaluate proposed contrast-agent dosing, administration duration, repeat study visits, and alternative agents before approving their use. Establish criteria for pausing or discontinuing a procedure and escalating medical concerns. Participant Evaluation & Medical Orders Establish a pre-participation medical screening and clearance process. Review participant histories and determine when additional evaluation or exclusion is appropriate. Issue participant-specific prescriptions or medical orders for Lumason or other approved study agents when clinically appropriate and consistent with the authorized protocol. Remain available for clinical consultation, abnormal findings, and adverse reactions during study activities, according to an agreed coverage plan. Nursing Oversight & Emergency Readiness Establish clinical expectations for IV placement, contrast administration, participant observation, and documentation. Support training and competency assessment for participating nurses. Determine appropriate clinical staffing and monitoring requirements based on the approved procedures, participant risks, and study setting. Review emergency equipment, medications, response procedures, and transfer arrangements before study initiation. Research & IRB Support Review and contribute to the clinical portions of Institutional Review Board (IRB) submissions, informed consent materials, and protocol amendments. Collaborate with the research team and regulatory advisors to address clinical safety questions and applicable study requirements. If appointed PI, fulfill the investigator responsibilities required by the approved protocol, IRB, and applicable regulations, including appropriate delegation, oversight, and safety reporting. Review adverse events and protocol deviations and support corrective actions. Quality & Program Growth Participate in clinical quality reviews and periodic study meetings. Review clinical documentation and adherence to approved protocols. Assess clinical readiness before increasing participant volume, adding personnel, or expanding study activities. Exercise independent medical judgment and recommend protocol changes or suspension of activities when necessary for participant safety.
Required Qualifications
MD or DO with an active, unrestricted California medical license. Board certification in a specialty relevant to the proposed study and clinical responsibilities. Experience with IV contrast agents, ultrasound procedures, or closely related clinical care. Ability to evaluate research literature and develop evidence-informed clinical protocols. Experience recognizing and managing acute contrast reactions and other medical emergencies. Professional liability coverage appropriate to the accepted clinical and research responsibilities. Willingness to complete required human-subject protection and research training.
Preferred Qualifications
Background in radiology, neurology, emergency medicine, anesthesiology, or another relevant specialty. Experience with contrast-enhanced ultrasound or ultrasound contrast agents. Prior clinical research, IRB submission, or Principal Investigator experience. Experience supervising nursing teams and developing clinical safety programs. Engagement Expectations The initial engagement will focus on study review, protocol development, clinical input for IRB submission, and readiness for participant enrollment. Ongoing responsibilities will include medical oversight, clinical availability, safety review, and support for study expansion. Final hours, onsite requirements, coverage arrangements, compensation, and any PI appointment will be established after review of the complete study materials. Clinical activities will begin only after the required approvals and operational safeguards are in place. Pay: $125.00 - $140.00 per hour Expected hours: 2.0 – 8.0 per week
Benefits
Flexible schedule Work Location: Remote